| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318031.1 | 3077 | Missense Mutation | CAT,CGT | H492R | NP_001304960.1 |
| NM_020436.4 | 3077 | Missense Mutation | CAT,CGT | H929R | NP_065169.1 |
| XM_005260467.3 | 3077 | Intron | XP_005260524.1 | ||
| XM_011528921.2 | 3077 | Missense Mutation | CAT,CGT | H827R | XP_011527223.1 |
| XM_011528922.2 | 3077 | Missense Mutation | CAT,CGT | H827R | XP_011527224.1 |