ENST00000399820.8:c.678A>C
MANE Select
|
ENSP00000382717.3:p.Glu226Asp
|
|
ENST00000399820.7:c.678A>C
|
ENSP00000382717.3:p.Glu226Asp
|
|
ENST00000503697.5:c.*146A>C
|
ENSP00000423706.1:n.*146A>C
|
|
ENST00000505055.5:c.*259A>C
|
ENSP00000425949.1:n.*259A>C
|
|
ENST00000506503.1:c.678A>C
|
ENSP00000423491.1:p.Glu226Asp
|
|
ENST00000506869.5:c.*259A>C
|
ENSP00000424319.1:n.*259A>C
|
|
ENST00000511729.5:n.40+22665A>C
|
|
|
ENST00000512448.1:n.272A>C
|
|
|
NM_025132.3:c.678A>C
|
NP_079408.3:p.Glu226Asp
|
|
XM_011513724.1:c.678A>C
|
XP_011512026.1:p.Glu226Asp
|
|
XM_011513725.1:c.612A>C
|
XP_011512027.1:p.Glu204Asp
|
|
XM_011513726.1:c.198A>C
|
XP_011512028.1:p.Glu66Asp
|
|
XM_011513727.1:c.198A>C
|
XP_011512029.1:p.Glu66Asp
|
|
XM_011513728.1:c.198A>C
|
XP_011512030.1:p.Glu66Asp
|
|
XM_011513729.1:c.678A>C
|
XP_011512031.1:p.Glu226Asp
|
|
XR_925155.1:n.742A>C
|
|
|
NM_001317924.1:c.198A>C
|
NP_001304853.1:p.Glu66Asp
|
|
XM_011513725.2:c.612A>C
|
XP_011512027.1:p.Glu204Asp
|
|
XM_011513726.3:c.198A>C
|
XP_011512028.1:p.Glu66Asp
|
|
XM_017008501.1:c.198A>C
|
XP_016863990.1:p.Glu66Asp
|
|
XR_001741306.1:n.742A>C
|
|
|
XR_001741307.1:n.742A>C
|
|
|
XR_001741308.1:n.742A>C
|
|
|
XR_001741309.1:n.742A>C
|
|
|
XR_001741310.1:n.742A>C
|
|
|
XR_001741311.2:n.591A>C
|
|
|
XR_001741312.1:n.742A>C
|
|
|
NM_025132.4:c.678A>C
MANE Select
|
NP_079408.3:p.Glu226Asp
|
|
NM_001317924.2:c.198A>C
|
NP_001304853.1:p.Glu66Asp
|
|