| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010859.1 | 1028 | Missense Mutation | TCT,TGT | S193C | NP_001010859.1 |
| XM_011529922.2 | 1028 | Intron | XP_011528224.1 | ||
| XM_017028629.1 | 1028 | Intron | XP_016884118.1 | ||
| XM_017028630.1 | 1028 | Missense Mutation | TCT,TGT | S176C | XP_016884119.1 |
| XM_017028631.1 | 1028 | UTR 3 | XP_016884120.1 | ||
| XM_017028632.1 | 1028 | Intron | XP_016884121.1 |