| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001160354.1 | 900 | UTR 3 | NP_001153826.1 | ||
| NM_001160355.1 | 900 | Intron | NP_001153827.1 | ||
| NM_017527.3 | 900 | Missense Mutation | TCC,TTC | S79F | NP_059997.3 |
| XM_005250989.4 | 900 | Intron | XP_005251046.1 | ||
| XM_005250990.4 | 900 | UTR 3 | XP_005251047.1 |