| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278613.1 | 5685 | Intron | NP_001265542.1 | ||
| NM_001278615.1 | 5685 | Intron | NP_001265544.1 | ||
| NM_002587.4 | 5685 | Intron | NP_002578.2 | ||
| NM_032420.3 | 5685 | Silent Mutation | CCA,CCG | P1069P | NP_115796.2 |
| XM_005268452.2 | 5685 | Silent Mutation | CCA,CCG | P1113P | XP_005268509.1 |
| XM_005268454.4 | 5685 | Silent Mutation | CCA,CCG | P1113P | XP_005268511.1 |
| XM_005268455.2 | 5685 | Silent Mutation | CCA,CCG | P690P | XP_005268512.1 |
| XM_017009517.1 | 5685 | Silent Mutation | CCA,CCG | P690P | XP_016865006.1 |
| XM_017009518.1 | 5685 | Intron | XP_016865007.1 |