| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001136023.2 | 929 | Missense Mutation | CAC,CGC | H169R | NP_001129495.1 |
| NM_001261461.1 | 929 | Missense Mutation | CAC,CGC | H169R | NP_001248390.1 |
| NM_006163.2 | 929 | Missense Mutation | CAC,CGC | H169R | NP_006154.1 |
| XM_005268906.4 | 929 | Missense Mutation | CAC,CGC | H169R | XP_005268963.1 |