| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001099222.1 | 998 | Intron | NP_001092692.1 | ||
| NM_001099223.1 | 998 | Intron | NP_001092693.1 | ||
| NM_001099224.1 | 998 | Intron | NP_001092694.1 | ||
| NM_025103.2 | 998 | Intron | NP_079379.2 | ||
| XM_011518035.2 | 998 | Intron | XP_011516337.1 | ||
| XM_011518036.2 | 998 | Intron | XP_011516338.1 | ||
| XM_017015163.1 | 998 | Intron | XP_016870652.1 | ||
| XM_017015164.1 | 998 | Intron | XP_016870653.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_022901.2 | 998 | Missense Mutation | TCG,TGG | S296W | NP_075052.1 |