| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256124.1 | 1299 | Missense Mutation | TGC,TTC | C399F | NP_001243053.1 |
| NM_173547.3 | 1299 | Missense Mutation | TGC,TTC | C421F | NP_775818.2 |
| XM_006721760.3 | 1299 | Missense Mutation | TGC,TTC | C434F | XP_006721823.1 |
| XM_006721761.3 | 1299 | Missense Mutation | TGC,TTC | C412F | XP_006721824.1 |
| XM_011524499.2 | 1299 | Intron | XP_011522801.1 | ||
| XM_011524500.2 | 1299 | Intron | XP_011522802.1 | ||
| XM_011524501.2 | 1299 | Intron | XP_011522803.1 | ||
| XM_011524502.2 | 1299 | Intron | XP_011522804.1 | ||
| XM_011524503.2 | 1299 | Intron | XP_011522805.1 | ||
| XM_017024343.1 | 1299 | Intron | XP_016879832.1 | ||
| XM_017024344.1 | 1299 | UTR 3 | XP_016879833.1 |