| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308006.1 | 334 | Missense Mutation | GCG,GTG | A19V | NP_001294935.1 |
| NM_006033.3 | 334 | Missense Mutation | GCG,GTG | A19V | NP_006024.1 |
| XM_005258390.1 | 334 | Intron | XP_005258447.1 | ||
| XM_011526265.2 | 334 | Intron | XP_011524567.1 | ||
| XM_011526267.1 | 334 | Intron | XP_011524569.1 | ||
| XM_017026095.1 | 334 | Intron | XP_016881584.1 |