| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184731.2 | 249 | Missense Mutation | CAT,CGT | H77R | NP_001171660.1 |
| NM_021081.5 | 249 | Missense Mutation | CAT,CGT | H77R | NP_066567.1 |
| XM_011528784.2 | 249 | Missense Mutation | CAT,CGT | H77R | XP_011527086.1 |
| XM_011528788.2 | 249 | Missense Mutation | CAT,CGT | H77R | XP_011527090.1 |