Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001103160.1 | 1198 | Missense Mutation | GCG,GTG | A289V | NP_001096630.1 |
NM_001103161.1 | 1198 | Missense Mutation | GCG,GTG | A373V | NP_001096631.1 |
XM_011541459.1 | 1198 | Missense Mutation | GCG,GTG | A373V | XP_011539761.1 |
XM_011541460.1 | 1198 | Missense Mutation | GCG,GTG | A373V | XP_011539762.1 |
XM_011541461.2 | 1198 | Missense Mutation | GCG,GTG | A373V | XP_011539763.1 |
XM_011541462.1 | 1198 | Missense Mutation | GCG,GTG | A372V | XP_011539764.1 |