| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098835.1 | 292 | Silent Mutation | CCA,CCG | P24P | NP_001092305.1 |
| NM_001278242.1 | 292 | Silent Mutation | CCA,CCG | P24P | NP_001265171.1 |
| NM_152717.2 | 292 | Intron | NP_689930.1 | ||
| XM_006718459.3 | 292 | Intron | XP_006718522.1 | ||
| XM_011544812.2 | 292 | Silent Mutation | CCA,CCG | P24P | XP_011543114.1 |
| XM_011544814.1 | 292 | UTR 5 | XP_011543116.1 |