PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
1901689-5	1991	We now report the results of sequencing of the entire coding region and exon-intron junctions of TBG-Quebec, which revealed two nucleotide substitutions; one, located in exon 3, changes the normal codon 283 of TTG (leucine) to that of TTT (phenylalanine), and the other, in exon 4, results in the replacement of the normal histidine-331 (CAT) by tyrosine (TAT).	Leucine	215-222	serpin family A member 7	Homo sapiens	97-100	
9510125-5	1998	Sequencing of the exons encoding the mature protein, adjacent introns and the promoter region, revealed differences in two nucleotides compared to the common type TBG, both located in exon 3: TGG (Trp) TAG (Stop) at codon 280 and TTG (Leu) TTT (Phe) at codon 283.	Leucine	235-238	serpin family A member 7	Homo sapiens	163-166	
7951486-8	1993	The sequencing of the entire coding exons and exon/intron junctions of TBG allele of the propositus revealed a single nucleotide substitution: CCT (proline) to CTT (leucine) at amino acid 363 of the TBG-C.	Leucine	165-172	serpin family A member 7	Homo sapiens	71-74	
1294376-5	1992	A single nucleotide substitution in the codon for the amino acid 363 of native TBG molecule (CCT to CTT) was found, resulting in the replacement of proline by leucine.	Leucine	159-166	serpin family A member 7	Homo sapiens	79-82	
2155256-6	1990	The Leu----Phe substitution, a relatively conservative replacement, is a TBG polymorphism present in 16% (3 of 19) of French Canadian males.	Leucine	4-7	serpin family A member 7	Homo sapiens	73-76