| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000456.2 | 991 | Missense Mutation | CAC,CGC | H40R | NP_000447.2 |
| NM_001032386.1 | 991 | Missense Mutation | CAC,CGC | H40R | NP_001027558.1 |
| NM_001032387.1 | 991 | Missense Mutation | CAC,CGC | H40R | NP_001027559.1 |
| XM_005269112.1 | 991 | Missense Mutation | CAC,CGC | H47R | XP_005269169.1 |
| XM_017019905.1 | 991 | Missense Mutation | CAC,CGC | H47R | XP_016875394.1 |
| XM_017019906.1 | 991 | Missense Mutation | CAC,CGC | H47R | XP_016875395.1 |
| XM_017019907.1 | 991 | Missense Mutation | CAC,CGC | H40R | XP_016875396.1 |
| XM_017019908.1 | 991 | Missense Mutation | CAC,CGC | H40R | XP_016875397.1 |