| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321395.1 | 1579 | Missense Mutation | TCC,TTC | S456F | NP_001308324.1 |
| NM_152781.3 | 1579 | Missense Mutation | TCC,TTC | S496F | NP_689994.2 |
| XM_005278233.2 | 1579 | Missense Mutation | TCC,TTC | S462F | XP_005278290.1 |
| XM_005278235.1 | 1579 | Missense Mutation | TCC,TTC | S422F | XP_005278292.1 |
| XM_006721802.3 | 1579 | Missense Mutation | TCC,TTC | S314F | XP_006721865.1 |
| XM_011524586.2 | 1579 | Missense Mutation | TCC,TTC | S462F | XP_011522888.1 |
| XM_017024424.1 | 1579 | Intron | XP_016879913.1 |