| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135772.1 | 3668 | Missense Mutation | TCG,TGG | S181W | NP_001129244.1 |
| NM_182492.2 | 3668 | Intron | NP_872298.1 | ||
| XM_006724372.3 | 3668 | Missense Mutation | TCG,TGG | S181W | XP_006724435.1 |
| XM_017029083.1 | 3668 | Missense Mutation | TCG,TGG | S181W | XP_016884572.1 |
| XM_017029084.1 | 3668 | Missense Mutation | TCG,TGG | S181W | XP_016884573.1 |
| XM_017029085.1 | 3668 | Missense Mutation | TCG,TGG | S181W | XP_016884574.1 |
| XM_017029086.1 | 3668 | Missense Mutation | TCG,TGG | S181W | XP_016884575.1 |
| XM_017029087.1 | 3668 | Missense Mutation | TCG,TGG | S181W | XP_016884576.1 |
| XM_017029088.1 | 3668 | Missense Mutation | TCG,TGG | S181W | XP_016884577.1 |