Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002017.2 | 441 | Intron | NP_001002017.1 | ||
NM_001002018.2 | 441 | Intron | NP_001002018.1 | ||
NM_001288665.1 | 441 | Intron | NP_001275594.1 | ||
NM_001288666.1 | 441 | Intron | NP_001275595.1 | ||
NM_001288667.1 | 441 | Intron | NP_001275596.1 | ||
NM_001288668.1 | 441 | Intron | NP_001275597.1 | ||
NM_001308070.1 | 441 | Intron | NP_001294999.1 | ||
NM_017885.3 | 441 | Intron | NP_060355.1 | ||
XM_011522559.2 | 441 | Intron | XP_011520861.1 | ||
XM_017023384.1 | 441 | Intron | XP_016878873.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016639.2 | 441 | Missense Mutation | AGA,GGA | R119G | NP_057723.1 |