| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256835.1 | 158 | Missense Mutation | TGG,TGT | W24C | NP_001243764.1 |
| NM_001256836.1 | 158 | Intron | NP_001243765.1 | ||
| NM_001256837.1 | 158 | Intron | NP_001243766.1 | ||
| NM_024638.3 | 158 | Missense Mutation | TGG,TGT | W12C | NP_078914.1 |
| XM_005247769.3 | 158 | Intron | XP_005247826.1 | ||
| XM_005247770.3 | 158 | UTR 5 | XP_005247827.1 | ||
| XM_006713744.3 | 158 | Intron | XP_006713807.1 | ||
| XM_011513137.2 | 158 | Missense Mutation | TGG,TGT | W24C | XP_011511439.1 |
| XM_017007182.1 | 158 | UTR 5 | XP_016862671.1 | ||
| XM_017007183.1 | 158 | Intron | XP_016862672.1 | ||
| XM_017007184.1 | 158 | UTR 5 | XP_016862673.1 |