| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001166271.2 | 495 | Intron | NP_001159743.1 | ||
| NM_001286792.1 | 495 | Missense Mutation | CCT,CGT | P10R | NP_001273721.1 |
| NM_001286793.1 | 495 | Intron | NP_001273722.1 | ||
| NM_001286794.1 | 495 | Intron | NP_001273723.1 | ||
| NM_001286795.1 | 495 | Intron | NP_001273724.1 | ||
| NM_153023.3 | 495 | Intron | NP_694568.1 |