| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_016470.7 | 592 | Missense Mutation | GCG,GTG | A99V | NP_057554.4 |
| XM_011528851.1 | 592 | Missense Mutation | GCG,GTG | A99V | XP_011527153.1 |
| XM_011528853.2 | 592 | Missense Mutation | GCG,GTG | A99V | XP_011527155.1 |
| XM_011528854.2 | 592 | Missense Mutation | GCG,GTG | A61V | XP_011527156.1 |
| XM_017027873.1 | 592 | Missense Mutation | GCG,GTG | A99V | XP_016883362.1 |