| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321307.1 | 5023 | Missense Mutation | AGT,TGT | S1393C | NP_001308236.1 |
| NM_002519.2 | 5023 | Missense Mutation | AGT,TGT | S1386C | NP_002510.2 |
| XM_011542854.2 | 5023 | Missense Mutation | AGT,TGT | S1395C | XP_011541156.1 |
| XM_017017802.1 | 5023 | Missense Mutation | AGT,TGT | S1327C | XP_016873291.1 |
| XM_017017803.1 | 5023 | Missense Mutation | AGT,TGT | S1327C | XP_016873292.1 |