| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281297.1 | 488 | Intron | NP_001268226.1 | ||
| NM_001281298.1 | 488 | Intron | NP_001268227.1 | ||
| NM_001281299.1 | 488 | Intron | NP_001268228.1 | ||
| NM_003792.3 | 488 | Intron | NP_003783.1 | ||
| NM_153200.2 | 488 | Missense Mutation | CAG,CGG | Q137R | NP_694880.1 |