| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282190.1 | 1798 | Missense Mutation | CAC,CGC | H383R | NP_001269119.1 |
| NM_001282191.1 | 1798 | Intron | NP_001269120.1 | ||
| NM_016478.4 | 1798 | Missense Mutation | CAC,CGC | H404R | NP_057562.3 |
| XM_005250403.2 | 1798 | Missense Mutation | CAC,CGC | H280R | XP_005250460.1 |
| XM_011516288.2 | 1798 | Missense Mutation | CAC,CGC | H337R | XP_011514590.1 |
| XM_011516289.2 | 1798 | Missense Mutation | CAC,CGC | H314R | XP_011514591.1 |
| XM_011516290.2 | 1798 | Missense Mutation | CAC,CGC | H236R | XP_011514592.1 |
| XM_017012287.1 | 1798 | Missense Mutation | CAC,CGC | H361R | XP_016867776.1 |
| XM_017012288.1 | 1798 | Missense Mutation | CAC,CGC | H236R | XP_016867777.1 |