Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001258248.1 | 707 | Missense Mutation | ATC,GTC | I156V | NP_001245177.1 |
NM_199262.2 | 707 | Missense Mutation | ATC,GTC | I156V | NP_954871.1 |
XM_006722115.3 | 707 | Missense Mutation | ATC,GTC | I156V | XP_006722178.1 |