Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001100607.2 | 1622 | Missense Mutation | ACA,GCA | T386A | NP_001094077.1 |
NM_016186.2 | 1622 | Missense Mutation | ACA,GCA | T386A | NP_057270.1 |
XM_005267733.4 | 1622 | Missense Mutation | ACA,GCA | T386A | XP_005267790.1 |
XM_017021353.1 | 1622 | Missense Mutation | ACA,GCA | T426A | XP_016876842.1 |