| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001163474.1 | 2170 | Missense Mutation | GCG,GTG | A591V | NP_001156946.1 |
| NM_152557.4 | 2170 | Missense Mutation | GCG,GTG | A590V | NP_689770.3 |
| XM_005249955.2 | 2170 | Missense Mutation | GCG,GTG | A606V | XP_005250012.1 |
| XM_005249956.2 | 2170 | Missense Mutation | GCG,GTG | A605V | XP_005250013.1 |
| XM_005249957.1 | 2170 | Missense Mutation | GCG,GTG | A593V | XP_005250014.1 |
| XM_011515838.1 | 2170 | Missense Mutation | GCG,GTG | A578V | XP_011514140.1 |