| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001267585.1 | 2632 | Intron | NP_001254514.1 | ||
| NM_001267586.1 | 2632 | Intron | NP_001254515.1 | ||
| XM_011523625.1 | 2632 | Intron | XP_011521927.1 | ||
| XM_011523626.2 | 2632 | Intron | XP_011521928.1 | ||
| XM_017024020.1 | 2632 | Silent Mutation | CGA,CGG | R800R | XP_016879509.1 |
| XM_017024021.1 | 2632 | UTR 3 | XP_016879510.1 |