| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195214.1 | 425 | Intron | NP_001182143.1 | ||
| NM_173834.3 | 425 | Missense Mutation | CAG,CGG | Q47R | NP_776195.2 |
| XM_011530923.2 | 425 | Missense Mutation | CAG,CGG | Q47R | XP_011529225.1 |
| XM_011530924.1 | 425 | Missense Mutation | CAG,CGG | Q6R | XP_011529226.1 |
| XM_017029450.1 | 425 | Missense Mutation | CAG,CGG | Q6R | XP_016884939.1 |
| XM_017029451.1 | 425 | Intron | XP_016884940.1 |