PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16029119-3	2005	Mutations in six exons (10, 11, 13, 14, 15, and 16) located in either cysteine-rich or tyrosine kinase domains cause one of three distinctive clinical subtypes: familial MTC, multiple endocrine neoplasia (MEN) type 2A (including variants with Hirschsprung"s disease and cutaneous lichen amyloidosis), and MEN 2B.	Cysteine	70-78	ret proto-oncogene	Homo sapiens	305-311