| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001144891.1 | 899 | Silent Mutation | CAC,CAG | H294Q | NP_001138363.1 |
| NM_001308110.1 | 899 | Intron | NP_001295039.1 | ||
| NM_016586.2 | 899 | Silent Mutation | CAC,CAG | H294Q | NP_057670.2 |
| XM_005267754.3 | 899 | Missense Mutation | CAC,CAG | H272Q | XP_005267811.1 |
| XM_005267756.4 | 899 | Intron | XP_005267813.1 | ||
| XM_017021367.1 | 899 | Intron | XP_016876856.1 |