Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317926.1 | 775 | Intron | NP_001304855.1 | ||
NM_013355.4 | 775 | Intron | NP_037487.2 | ||
XM_005251946.3 | 775 | Intron | XP_005252003.1 | ||
XM_006717080.2 | 775 | Intron | XP_006717143.1 | ||
XM_017014649.1 | 775 | Intron | XP_016870138.1 | ||
XM_017014650.1 | 775 | Intron | XP_016870139.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318015.1 | 775 | Missense Mutation | CCG,CTG | P251L | NP_001304944.1 |
NM_001318016.1 | 775 | Silent Mutation | CCC,CCT | P205P | NP_001304945.1 |
NM_001318020.1 | 775 | Missense Mutation | CGC,TGC | R189C | NP_001304949.1 |
NM_001318023.1 | 775 | Missense Mutation | CCG,CTG | P195L | NP_001304952.1 |
NM_032799.4 | 775 | Missense Mutation | CCG,CTG | P196L | NP_116188.2 |
XM_011519116.2 | 775 | Missense Mutation | CGC,TGC | R244C | XP_011517418.1 |