| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300928.1 | 572 | Missense Mutation | CAA,CGA | Q78R | NP_001287857.1 |
| NM_001300929.1 | 572 | Missense Mutation | CAA,CGA | Q56R | NP_001287858.1 |
| NM_003795.5 | 572 | Missense Mutation | CAA,CGA | Q78R | NP_003786.1 |
| NM_152827.3 | 572 | Intron | NP_690040.1 |