| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304428.1 | 632 | Missense Mutation | CAT,CGT | H36R | NP_001291357.1 |
| NM_001304429.1 | 632 | Missense Mutation | CAT,CGT | H36R | NP_001291358.1 |
| NM_001304431.1 | 632 | Missense Mutation | CAT,CGT | H36R | NP_001291360.1 |
| NM_152687.3 | 632 | Missense Mutation | CAT,CGT | H36R | NP_689900.1 |