| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000578.3 | 675 | Silent Mutation | CCA,CCG | P24P | NP_000569.3 |
| XM_005246793.3 | 675 | Intron | XP_005246850.1 | ||
| XM_005246794.3 | 675 | UTR 5 | XP_005246851.1 | ||
| XM_006712709.3 | 675 | Intron | XP_006712772.1 | ||
| XM_006712710.3 | 675 | Intron | XP_006712773.1 | ||
| XM_006712711.3 | 675 | Intron | XP_006712774.1 | ||
| XM_011511684.2 | 675 | UTR 5 | XP_011509986.1 | ||
| XM_011511685.2 | 675 | Intron | XP_011509987.1 | ||
| XM_017004765.1 | 675 | Silent Mutation | CCA,CCG | P24P | XP_016860254.1 |
| XM_017004766.1 | 675 | UTR 5 | XP_016860255.1 | ||
| XM_017004767.1 | 675 | Silent Mutation | CCA,CCG | P24P | XP_016860256.1 |