Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130964.1 | 2612 | Missense Mutation | CAG,CGG | Q763R | NP_001124436.1 |
NM_006225.3 | 2612 | Missense Mutation | CAG,CGG | Q742R | NP_006216.2 |
XM_017006622.1 | 2612 | Missense Mutation | CAG,CGG | Q684R | XP_016862111.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015873.3 | 2612 | Intron | NP_056957.3 | ||
XM_005265191.3 | 2612 | Intron | XP_005265248.1 | ||
XM_005265192.4 | 2612 | Intron | XP_005265249.1 | ||
XM_006713184.3 | 2612 | Intron | XP_006713247.1 | ||
XM_011533770.2 | 2612 | Intron | XP_011532072.1 | ||
XM_011533771.1 | 2612 | Intron | XP_011532073.1 | ||
XM_011533773.2 | 2612 | Intron | XP_011532075.1 |