| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001764.2 | 557 | Intron | NP_001755.1 | ||
| XM_011510119.2 | 557 | Intron | XP_011508421.1 | ||
| XM_017002784.1 | 557 | Intron | XP_016858273.1 | ||
| XM_017002785.1 | 557 | Intron | XP_016858274.1 | ||
| XM_017002786.1 | 557 | Intron | XP_016858275.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001765.2 | 557 | Missense Mutation | CGT,TGT | R89C | NP_001756.2 |
| XM_005245579.4 | 557 | Missense Mutation | CGT,TGT | R89C | XP_005245636.1 |