| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001173473.1 | 1622 | Missense Mutation | AGC,TGC | S466C | NP_001166944.1 |
| NM_001173474.1 | 1622 | Missense Mutation | AGC,TGC | S508C | NP_001166945.1 |
| NM_004192.3 | 1622 | Missense Mutation | AGC,TGC | S524C | NP_004183.2 |
| XM_005274434.3 | 1622 | Missense Mutation | AGC,TGC | S524C | XP_005274491.1 |
| XM_011546185.2 | 1622 | Missense Mutation | AGC,TGC | S441C | XP_011544487.1 |
| XM_017029919.1 | 1622 | Missense Mutation | AGC,TGC | S415C | XP_016885408.1 |