| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171201.1 | 35 | Missense Mutation | AGG,TGG | R9W | NP_001164672.1 |
| NM_001171202.1 | 35 | Missense Mutation | AGG,TGG | R9W | NP_001164673.1 |
| NM_001171203.2 | 35 | UTR 5 | NP_001164674.1 | ||
| NM_001171204.2 | 35 | UTR 5 | NP_001164675.1 | ||
| NM_016525.4 | 35 | UTR 5 | NP_057609.2 | ||
| XM_006716779.3 | 35 | Intron | XP_006716842.1 | ||
| XM_011517898.2 | 35 | Intron | XP_011516200.1 | ||
| XM_011517899.1 | 35 | Intron | XP_011516201.1 | ||
| XM_011517900.1 | 35 | Intron | XP_011516202.1 | ||
| XM_017014801.1 | 35 | Intron | XP_016870290.1 | ||
| XM_017014802.1 | 35 | Intron | XP_016870291.1 |