| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303245.1 | 63 | Missense Mutation | GCG,GTG | A9V | NP_001290174.1 |
| NM_001303246.1 | 63 | Missense Mutation | GCG,GTG | A9V | NP_001290175.1 |
| NM_006506.3 | 63 | Missense Mutation | GCG,GTG | A9V | NP_006497.2 |
| XM_011513059.2 | 63 | Intron | XP_011511361.1 | ||
| XM_017006968.1 | 63 | Intron | XP_016862457.1 | ||
| XM_017006969.1 | 63 | Intron | XP_016862458.1 | ||
| XM_017006970.1 | 63 | Intron | XP_016862459.1 | ||
| XM_017006971.1 | 63 | Intron | XP_016862460.1 | ||
| XM_017006972.1 | 63 | Intron | XP_016862461.1 |