| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195124.1 | 634 | Silent Mutation | GCA,GCG | A212A | NP_001182053.1 |
| NM_001195125.1 | 634 | Missense Mutation | CAC,CGC | H151R | NP_001182054.1 |
| NM_001256917.1 | 634 | Missense Mutation | CAC,CGC | H136R | NP_001243846.1 |