| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000835.4 | 4312 | Silent Mutation | CCA,CCG | P955P | NP_000826.2 |
| NM_001278553.1 | 4312 | Intron | NP_001265482.1 | ||
| XM_006721845.3 | 4312 | Silent Mutation | CCA,CCG | P1030P | XP_006721908.1 |
| XM_006721846.3 | 4312 | Silent Mutation | CCA,CCG | P1029P | XP_006721909.1 |
| XM_011524686.2 | 4312 | Silent Mutation | CCA,CCG | P1058P | XP_011522988.1 |
| XM_011524687.2 | 4312 | Silent Mutation | CCA,CCG | P1051P | XP_011522989.1 |
| XM_011524688.2 | 4312 | Silent Mutation | CCA,CCG | P1038P | XP_011522990.1 |
| XM_011524689.2 | 4312 | Silent Mutation | CCA,CCG | P984P | XP_011522991.1 |
| XM_011524692.2 | 4312 | Intron | XP_011522994.1 | ||
| XM_017024544.1 | 4312 | Silent Mutation | CCA,CCG | P1059P | XP_016880033.1 |