| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001017396.2 | 713 | Missense Mutation | CAT,CTT | H35L | NP_001017396.1 |
| NM_001282398.1 | 713 | Intron | NP_001269327.1 | ||
| NM_001291604.1 | 713 | Intron | NP_001278533.1 | ||
| NM_001291605.1 | 713 | Missense Mutation | CAT,CTT | H77L | NP_001278534.1 |
| NM_021088.3 | 713 | Missense Mutation | CAT,CTT | H77L | NP_066574.2 |