| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184801.1 | 588 | Missense Mutation | CAT,CGT | H97R | NP_001171730.1 |
| NM_015255.2 | 588 | Missense Mutation | CAT,CGT | H97R | NP_056070.1 |
| XM_005248965.4 | 588 | Missense Mutation | CAT,CGT | H97R | XP_005249022.1 |
| XM_005248966.3 | 588 | Intron | XP_005249023.1 | ||
| XM_011514438.2 | 588 | Missense Mutation | CAT,CGT | H124R | XP_011512740.2 |
| XM_011514439.1 | 588 | Intron | XP_011512741.1 | ||
| XM_011514440.1 | 588 | Intron | XP_011512742.1 | ||
| XM_011514441.2 | 588 | Intron | XP_011512743.1 | ||
| XM_017010594.1 | 588 | Missense Mutation | CAT,CGT | H124R | XP_016866083.1 |
| XM_017010595.1 | 588 | Missense Mutation | CAT,CGT | H124R | XP_016866084.1 |
| XM_017010596.1 | 588 | Missense Mutation | CAT,CGT | H97R | XP_016866085.1 |
| XM_017010597.1 | 588 | Missense Mutation | CAT,CGT | H124R | XP_016866086.1 |