| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017741.3 | 1052 | Missense Mutation | TCT,TGT | S36C | NP_060211.3 |
| XM_005248169.3 | 1052 | Missense Mutation | TCT,TGT | S36C | XP_005248226.1 |
| XM_005248171.3 | 1052 | Missense Mutation | TCT,TGT | S36C | XP_005248228.1 |
| XM_006713966.3 | 1052 | Missense Mutation | TCT,TGT | S36C | XP_006714029.1 |
| XM_017008327.1 | 1052 | Missense Mutation | TCT,TGT | S36C | XP_016863816.1 |
| XM_017008328.1 | 1052 | Missense Mutation | TCT,TGT | S36C | XP_016863817.1 |