| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278531.1 | 200 | Intron | NP_001265460.1 | ||
| NM_001278532.1 | 200 | Intron | NP_001265461.1 | ||
| NM_001278533.1 | 200 | Intron | NP_001265462.1 | ||
| NM_018341.2 | 200 | Intron | NP_060811.1 | ||
| XM_011535938.2 | 200 | Intron | XP_011534240.1 | ||
| XM_011535939.2 | 200 | Intron | XP_011534241.1 | ||
| XM_011535940.2 | 200 | Intron | XP_011534242.1 | ||
| XM_017011027.1 | 200 | Intron | XP_016866516.1 | ||
| XM_017011028.1 | 200 | Intron | XP_016866517.1 | ||
| XM_017011029.1 | 200 | Intron | XP_016866518.1 | ||
| XM_017011030.1 | 200 | Intron | XP_016866519.1 | ||
| XM_017011031.1 | 200 | Intron | XP_016866520.1 | ||
| XM_017011032.1 | 200 | Intron | XP_016866521.1 | ||
| XM_017011033.1 | 200 | Intron | XP_016866522.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| XM_006715554.3 | 200 | Missense Mutation | ACG,ATG | T26M | XP_006715617.1 |
| XM_011536093.2 | 200 | Missense Mutation | ACG,ATG | T26M | XP_011534395.1 |