| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_033063.1 | 4263 | Silent Mutation | CCA,CCG | P537P | NP_149052.1 |
| NM_207577.1 | 4263 | Intron | NP_997460.1 | ||
| XM_006718556.3 | 4263 | Intron | XP_006718619.1 | ||
| XM_011545039.2 | 4263 | Intron | XP_011543341.1 | ||
| XM_017017755.1 | 4263 | Silent Mutation | CCA,CCG | P553P | XP_016873244.1 |
| XM_017017756.1 | 4263 | Silent Mutation | CCA,CCG | P252P | XP_016873245.1 |
| XM_017017757.1 | 4263 | Silent Mutation | CCA,CCG | P236P | XP_016873246.1 |
| XM_017017758.1 | 4263 | Silent Mutation | CCA,CCG | P224P | XP_016873247.1 |