ENST00000682424.1:c.292G>A
|
ENSP00000507321.1:p.Ala98Thr
|
|
ENST00000299427.12:c.406G>A
MANE Select
|
ENSP00000299427.6:p.Ala136Thr
|
|
ENST00000428886.7:n.494G>A
|
|
|
ENST00000436873.7:c.210G>A
|
|
|
ENST00000524788.2:n.1418G>A
|
|
|
ENST00000524903.2:n.1534G>A
|
|
|
ENST00000528571.6:c.*146G>A
|
ENSP00000434647.1:n.*146G>A
|
|
ENST00000528807.2:n.62G>A
|
|
|
ENST00000530040.2:n.435G>A
|
|
|
ENST00000533371.6:c.-324G>A
|
ENSP00000437066.1:n.-324G>A
|
|
ENST00000534644.6:n.407G>A
|
|
|
ENST00000642892.1:c.-271G>A
|
ENSP00000494165.1:n.-271G>A
|
|
ENST00000643439.1:c.*146G>A
|
ENSP00000495849.1:n.*146G>A
|
|
ENST00000643479.1:n.435G>A
|
|
|
ENST00000643516.1:c.293G>A
|
|
|
ENST00000644151.1:n.1698G>A
|
|
|
ENST00000644218.1:c.406G>A
|
ENSP00000493574.1:p.Ala136Thr
|
|
ENST00000644683.1:c.406G>A
|
ENSP00000494085.1:p.Ala136Thr
|
|
ENST00000644810.1:c.230-250G>A
|
ENSP00000495895.1:n.230-250G>A
|
|
ENST00000644831.1:n.435G>A
|
|
|
ENST00000644933.1:c.-324G>A
|
ENSP00000496133.1:n.-324G>A
|
|
ENST00000645020.1:n.1434G>A
|
|
|
ENST00000645285.1:c.-324G>A
|
ENSP00000495058.1:n.-324G>A
|
|
ENST00000645331.1:n.625G>A
|
|
|
ENST00000645620.1:c.-266G>A
|
ENSP00000493657.1:n.-266G>A
|
|
ENST00000646777.1:n.435G>A
|
|
|
ENST00000647016.1:n.739G>A
|
|
|
ENST00000647152.1:c.-324G>A
|
ENSP00000495893.1:n.-324G>A
|
|
ENST00000647209.1:c.*275G>A
|
ENSP00000495558.1:n.*275G>A
|
|
ENST00000647346.1:n.1426G>A
|
|
|
ENST00000299427.10:c.406G>A
|
ENSP00000299427.6:p.Ala136Thr
|
|
ENST00000428886.6:n.428G>A
|
|
|
ENST00000436873.6:c.406G>A
|
ENSP00000398136.2:p.Ala136Thr
|
|
ENST00000528571.5:c.*146G>A
|
ENSP00000434647.1:n.*146G>A
|
|
ENST00000530040.1:n.518G>A
|
|
|
ENST00000533371.5:c.-324G>A
|
ENSP00000437066.1:n.-324G>A
|
|
ENST00000534644.5:n.391G>A
|
|
|
ENST00000611494.4:c.406G>A
|
ENSP00000484546.1:p.Ala136Thr
|
|
NM_000391.3:c.406G>A
|
NP_000382.3:p.Ala136Thr
|
|
NM_000391.4:c.406G>A
MANE Select
|
NP_000382.3:p.Ala136Thr
|
|