| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005708.3 | 642 | Missense Mutation | AGG,TGG | R4W | NP_005699.1 |
| XM_011521044.2 | 642 | Intron | XP_011519346.1 | ||
| XM_017020298.1 | 642 | Intron | XP_016875787.1 | ||
| XM_017020299.1 | 642 | Intron | XP_016875788.1 | ||
| XM_017020300.1 | 642 | Intron | XP_016875789.1 | ||
| XM_017020301.1 | 642 | Intron | XP_016875790.1 | ||
| XM_017020302.1 | 642 | Intron | XP_016875791.1 |