| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001206960.1 | 98 | Missense Mutation | TCG,TGG | S11W | NP_001193889.1 |
| NM_001206961.1 | 98 | UTR 5 | NP_001193890.1 | ||
| NM_001293225.1 | 98 | Intron | NP_001280154.1 | ||
| NM_015900.3 | 98 | Missense Mutation | TCG,TGG | S11W | NP_056984.1 |
| XM_017006572.1 | 98 | UTR 5 | XP_016862061.1 |