| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006056.4 | 1354 | Missense Mutation | GCG,GTG | A419V | NP_006047.3 |
| XM_006712195.3 | 1354 | Intron | XP_006712258.1 | ||
| XM_006712196.3 | 1354 | Intron | XP_006712259.1 | ||
| XM_011510487.2 | 1354 | Missense Mutation | GCG,GTG | A396V | XP_011508789.1 |
| XM_011510488.2 | 1354 | Intron | XP_011508790.1 | ||
| XM_011510489.2 | 1354 | Intron | XP_011508791.1 |