Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001257370.1 | 999 | Intron | NP_001244299.1 | ||
XM_017023025.1 | 999 | Intron | XP_016878514.1 | ||
XM_017023026.1 | 999 | Intron | XP_016878515.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001324081.1 | 999 | Missense Mutation | CCG,CTG | P303L | NP_001311010.1 |
NM_080861.3 | 999 | Missense Mutation | CCG,CTG | P303L | NP_543137.2 |
XM_005255673.4 | 999 | Missense Mutation | CCG,CTG | P358L | XP_005255730.1 |