Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000413.2 | 1297 | Missense Mutation | GCG,GTG | A189V | NP_000404.2 |
XM_005257292.3 | 1297 | Missense Mutation | GCG,GTG | A220V | XP_005257349.1 |
XM_006721857.3 | 1297 | Missense Mutation | GCG,GTG | A221V | XP_006721920.1 |
XM_006721858.3 | 1297 | Missense Mutation | GCG,GTG | A220V | XP_006721921.1 |
XM_006721859.3 | 1297 | Missense Mutation | GCG,GTG | A221V | XP_006721922.1 |
XM_011524729.1 | 1297 | Missense Mutation | GCG,GTG | A190V | XP_011523031.1 |
XM_011524730.1 | 1297 | Missense Mutation | GCG,GTG | A189V | XP_011523032.1 |
XM_011524731.1 | 1297 | Missense Mutation | GCG,GTG | A190V | XP_011523033.1 |
XM_011524732.2 | 1297 | UTR 3 | XP_011523034.1 |