| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001161476.1 | 177 | Missense Mutation | CAT,CGT | H26R | NP_001154948.1 |
| NM_024515.4 | 177 | Missense Mutation | CAT,CGT | H26R | NP_078791.3 |
| XM_005268056.4 | 177 | Missense Mutation | CAT,CGT | H26R | XP_005268113.1 |
| XM_005268057.3 | 177 | Intron | XP_005268114.1 | ||
| XM_005268058.4 | 177 | Intron | XP_005268115.1 | ||
| XM_011537150.2 | 177 | Missense Mutation | CAT,CGT | H26R | XP_011535452.1 |
| XM_011537151.2 | 177 | Intron | XP_011535453.2 | ||
| XM_017021639.1 | 177 | Intron | XP_016877128.1 |