| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001294340.1 | 322 | Missense Mutation | GCG,GTG | A41V | NP_001281269.1 |
| NM_144604.3 | 322 | Missense Mutation | GCG,GTG | A41V | NP_653205.3 |
| XM_011522863.1 | 322 | Missense Mutation | GCG,GTG | A41V | XP_011521165.1 |
| XM_011522865.1 | 322 | Intron | XP_011521167.1 | ||
| XM_017022934.1 | 322 | Missense Mutation | GCG,GTG | A41V | XP_016878423.1 |