| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243342.1 | 535 | Silent Mutation | CCA,CCG | P168P | NP_001230271.1 |
| NM_017950.3 | 535 | Silent Mutation | CCA,CCG | P168P | NP_060420.2 |
| XM_005257492.4 | 535 | Silent Mutation | CCA,CCG | P168P | XP_005257549.1 |
| XM_011524963.2 | 535 | Silent Mutation | CCA,CCG | P138P | XP_011523265.1 |
| XM_011524964.2 | 535 | Intron | XP_011523266.1 | ||
| XM_011524965.2 | 535 | Silent Mutation | CCA,CCG | P168P | XP_011523267.1 |
| XM_017024807.1 | 535 | Silent Mutation | CCA,CCG | P168P | XP_016880296.1 |