| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001014437.2 | 2110 | Missense Mutation | GCG,GTG | A751V | NP_001014437.1 |
| NM_001194997.1 | 2110 | Missense Mutation | GCG,GTG | A751V | NP_001181926.1 |
| NM_001751.5 | 2110 | Missense Mutation | GCG,GTG | A668V | NP_001742.1 |
| NM_139273.3 | 2110 | Missense Mutation | GCG,GTG | A668V | NP_644802.1 |
| XM_006718341.3 | 2110 | Missense Mutation | GCG,GTG | A658V | XP_006718404.1 |
| XM_017018389.1 | 2110 | Missense Mutation | GCG,GTG | A658V | XP_016873878.1 |
| XM_017018390.1 | 2110 | Missense Mutation | GCG,GTG | A658V | XP_016873879.1 |
| XM_017018391.1 | 2110 | Missense Mutation | GCG,GTG | A576V | XP_016873880.1 |
| XM_017018392.1 | 2110 | Missense Mutation | GCG,GTG | A681V | XP_016873881.1 |