| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006822.2 | 852 | Missense Mutation | CCG,CGG | P205R | NP_006813.1 |
| XM_005256334.4 | 852 | Missense Mutation | CCG,CGG | P145R | XP_005256391.1 |
| XM_005256335.3 | 852 | Intron | XP_005256392.1 | ||
| XM_006722271.3 | 852 | Missense Mutation | CCG,CGG | P165R | XP_006722334.1 |
| XM_011523528.2 | 852 | Missense Mutation | CCG,CGG | P188R | XP_011521830.1 |
| XM_017024042.1 | 852 | Intron | XP_016879531.1 | ||
| XM_017024043.1 | 852 | Missense Mutation | CCG,CGG | P145R | XP_016879532.1 |