| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001178089.2 | 606 | Missense Mutation | TCT,TGT | S82C | NP_001171560.1 |
| NM_001178090.2 | 606 | Missense Mutation | TCT,TGT | S82C | NP_001171561.1 |
| NM_001323306.1 | 606 | Missense Mutation | TCT,TGT | S82C | NP_001310235.1 |
| NM_001323307.1 | 606 | Missense Mutation | TCT,TGT | S82C | NP_001310236.1 |
| NM_001323308.1 | 606 | Missense Mutation | TCT,TGT | S82C | NP_001310237.1 |
| NM_001323309.1 | 606 | Missense Mutation | TCT,TGT | S82C | NP_001310238.1 |
| NM_001323310.1 | 606 | Missense Mutation | TCT,TGT | S82C | NP_001310239.1 |
| NM_182594.3 | 606 | Missense Mutation | TCT,TGT | S82C | NP_872400.2 |