| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001291366.1 | 2048 | Missense Mutation | GCG,GTG | A777V | NP_001278295.1 |
| NM_001291367.1 | 2048 | Missense Mutation | GCG,GTG | A683V | NP_001278296.1 |
| XM_017002583.1 | 2048 | Missense Mutation | GCG,GTG | A777V | XP_016858072.1 |
| XM_017002584.1 | 2048 | Missense Mutation | GCG,GTG | A777V | XP_016858073.1 |
| XM_017002585.1 | 2048 | Missense Mutation | GCG,GTG | A755V | XP_016858074.1 |