| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014856.2 | 4520 | Missense Mutation | GCG,GTG | A1321V | NP_055671.2 |
| XM_005245678.4 | 4520 | Missense Mutation | GCG,GTG | A1332V | XP_005245735.1 |
| XM_005245679.2 | 4520 | Missense Mutation | GCG,GTG | A1321V | XP_005245736.1 |
| XM_011510219.1 | 4520 | Missense Mutation | GCG,GTG | A1249V | XP_011508521.1 |
| XM_011510220.2 | 4520 | Missense Mutation | GCG,GTG | A1216V | XP_011508522.1 |
| XM_011510221.2 | 4520 | Missense Mutation | GCG,GTG | A1119V | XP_011508523.1 |
| XM_011510222.1 | 4520 | Intron | XP_011508524.1 | ||
| XM_017002993.1 | 4520 | Missense Mutation | GCG,GTG | A1241V | XP_016858482.1 |