Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001042610.2 | 107 | Intron | NP_001036075.1 | ||
NM_001288708.1 | 107 | UTR 5 | NP_001275637.1 | ||
NM_001288709.1 | 107 | Missense Mutation | CGG,GGG | R32G | NP_001275638.1 |
NM_024043.3 | 107 | Intron | NP_076948.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286205.1 | 107 | Intron | NP_001273134.1 | ||
NM_001286208.1 | 107 | Intron | NP_001273137.1 | ||
NM_001286209.1 | 107 | Intron | NP_001273138.1 | ||
NM_001481.2 | 107 | Intron | NP_001472.1 | ||
XM_005256304.4 | 107 | Intron | XP_005256361.1 | ||
XM_005256309.4 | 107 | Intron | XP_005256366.1 | ||
XM_006721175.3 | 107 | Intron | XP_006721238.1 | ||
XM_011522990.2 | 107 | Intron | XP_011521292.1 | ||
XM_011522991.1 | 107 | Intron | XP_011521293.1 | ||
XM_011522992.2 | 107 | Intron | XP_011521294.1 | ||
XM_017023122.1 | 107 | Intron | XP_016878611.1 | ||
XM_017023123.1 | 107 | Intron | XP_016878612.1 | ||
XM_017023124.1 | 107 | Intron | XP_016878613.1 | ||
XM_017023125.1 | 107 | Intron | XP_016878614.1 |