| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000601.5 | 2161 | Missense Mutation | CAT,CGT | H645R | NP_000592.3 |
| NM_001010931.2 | 2161 | Intron | NP_001010931.1 | ||
| NM_001010932.2 | 2161 | Missense Mutation | CAT,CGT | H640R | NP_001010932.1 |
| NM_001010933.2 | 2161 | Intron | NP_001010933.1 | ||
| NM_001010934.2 | 2161 | Intron | NP_001010934.1 | ||
| XM_006715956.2 | 2161 | Missense Mutation | CAT,CGT | H645R | XP_006716019.1 |
| XM_011516115.2 | 2161 | Missense Mutation | CAT,CGT | H640R | XP_011514417.1 |
| XM_017012097.1 | 2161 | Intron | XP_016867586.1 | ||
| XM_017012098.1 | 2161 | Intron | XP_016867587.1 |