| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003561.2 | 826 | Missense Mutation | TCG,TTG | S161L | NP_003552.1 |
| XM_011522695.2 | 826 | Intron | XP_011520997.1 | ||
| XM_011522696.2 | 826 | Intron | XP_011520998.1 | ||
| XM_011522697.1 | 826 | Intron | XP_011520999.1 | ||
| XM_011522698.1 | 826 | Intron | XP_011521000.1 |