| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014299.2 | 4130 | Intron | NP_055114.1 | ||
| NM_058243.2 | 4130 | Missense Mutation | GCG,GTG | A1303V | NP_490597.1 |
| XM_011527854.1 | 4130 | Missense Mutation | GCG,GTG | A1303V | XP_011526156.1 |
| XM_011527855.1 | 4130 | Intron | XP_011526157.1 | ||
| XM_011527856.2 | 4130 | Intron | XP_011526158.1 |