| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000352.4 | 4861 | Missense Mutation | CGT,TGT | R1578C | NP_000343.2 |
| NM_001287174.1 | 4861 | Missense Mutation | CGT,TGT | R1579C | NP_001274103.1 |
| XM_011520331.2 | 4861 | Missense Mutation | CGT,TGT | R1578C | XP_011518633.1 |
| XM_017018197.1 | 4861 | Missense Mutation | CGT,TGT | R1601C | XP_016873686.1 |
| XM_017018198.1 | 4861 | Missense Mutation | CGT,TGT | R1600C | XP_016873687.1 |
| XM_017018199.1 | 4861 | Missense Mutation | CGT,TGT | R1600C | XP_016873688.1 |
| XM_017018200.1 | 4861 | Missense Mutation | CGT,TGT | R1577C | XP_016873689.1 |
| XM_017018201.1 | 4861 | Intron | XP_016873690.1 | ||
| XM_017018202.1 | 4861 | Missense Mutation | CGT,TGT | R1100C | XP_016873691.1 |
| XM_017018203.1 | 4861 | Intron | XP_016873692.1 | ||
| XM_017018204.1 | 4861 | Missense Mutation | CGT,TGT | R897C | XP_016873693.1 |