| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184745.1 | 785 | Intron | NP_001171674.1 | ||
| NM_033215.4 | 785 | Missense Mutation | GCG,GTG | A253V | NP_149992.3 |
| XM_005272687.3 | 785 | Missense Mutation | GCG,GTG | A253V | XP_005272744.1 |
| XM_017029932.1 | 785 | Intron | XP_016885421.1 | ||
| XM_017029933.1 | 785 | Intron | XP_016885422.1 | ||
| XM_017029934.1 | 785 | Missense Mutation | GCG,GTG | A253V | XP_016885423.1 |
| XM_017029935.1 | 785 | Missense Mutation | GCG,GTG | A253V | XP_016885424.1 |