| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001017523.1 | 1918 | Intron | NP_001017523.1 | ||
| NM_001018072.1 | 1918 | Missense Mutation | GGG,TGG | G49W | NP_001018082.1 |
| XM_005268645.3 | 1918 | Intron | XP_005268702.1 | ||
| XM_011537909.2 | 1918 | Intron | XP_011536211.1 | ||
| XM_011537910.2 | 1918 | Intron | XP_011536212.1 | ||
| XM_017018807.1 | 1918 | Missense Mutation | GGG,TGG | G49W | XP_016874296.1 |