| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002892.3 | 381 | Missense Mutation | GCG,GTG | A3V | NP_002883.3 |
| NM_023000.2 | 381 | Missense Mutation | GCG,GTG | A3V | NP_075376.2 |
| NM_023001.2 | 381 | Missense Mutation | GCG,GTG | A3V | NP_075377.2 |
| XM_005267964.2 | 381 | Missense Mutation | GCG,GTG | A3V | XP_005268021.1 |
| XM_005267965.2 | 381 | Missense Mutation | GCG,GTG | A3V | XP_005268022.1 |
| XM_017021560.1 | 381 | Missense Mutation | GCG,GTG | A3V | XP_016877049.1 |
| XM_017021561.1 | 381 | Missense Mutation | GCG,GTG | A3V | XP_016877050.1 |
| XM_017021562.1 | 381 | Missense Mutation | GCG,GTG | A3V | XP_016877051.1 |
| XM_017021563.1 | 381 | Missense Mutation | GCG,GTG | A3V | XP_016877052.1 |
| XM_017021564.1 | 381 | Intron | XP_016877053.1 | ||
| XM_017021565.1 | 381 | Intron | XP_016877054.1 |