|
ENST00000682424.1:c.326A>C
|
ENSP00000507321.1:p.Glu109Ala
|
|
|
ENST00000299427.12:c.440A>C
MANE Select
|
ENSP00000299427.6:p.Glu147Ala
|
|
|
ENST00000428886.7:n.528A>C
|
|
|
|
ENST00000436873.7:c.244A>C
|
|
|
|
ENST00000524788.2:n.1452A>C
|
|
|
|
ENST00000524903.2:n.1568A>C
|
|
|
|
ENST00000528571.6:c.*180A>C
|
ENSP00000434647.1:n.*180A>C
|
|
|
ENST00000528807.2:n.96A>C
|
|
|
|
ENST00000530040.2:n.469A>C
|
|
|
|
ENST00000533371.6:c.-290A>C
|
ENSP00000437066.1:n.-290A>C
|
|
|
ENST00000534644.6:n.441A>C
|
|
|
|
ENST00000642892.1:c.-237A>C
|
ENSP00000494165.1:n.-237A>C
|
|
|
ENST00000643439.1:c.*180A>C
|
ENSP00000495849.1:n.*180A>C
|
|
|
ENST00000643479.1:n.469A>C
|
|
|
|
ENST00000643516.1:c.327A>C
|
|
|
|
ENST00000644151.1:n.1732A>C
|
|
|
|
ENST00000644218.1:c.440A>C
|
ENSP00000493574.1:p.Glu147Ala
|
|
|
ENST00000644683.1:c.440A>C
|
ENSP00000494085.1:p.Glu147Ala
|
|
|
ENST00000644810.1:c.230-216A>C
|
ENSP00000495895.1:n.230-216A>C
|
|
|
ENST00000644831.1:n.469A>C
|
|
|
|
ENST00000644933.1:c.-290A>C
|
ENSP00000496133.1:n.-290A>C
|
|
|
ENST00000645020.1:n.1468A>C
|
|
|
|
ENST00000645285.1:c.-290A>C
|
ENSP00000495058.1:n.-290A>C
|
|
|
ENST00000645331.1:n.659A>C
|
|
|
|
ENST00000645620.1:c.-232A>C
|
ENSP00000493657.1:n.-232A>C
|
|
|
ENST00000646777.1:n.469A>C
|
|
|
|
ENST00000647016.1:n.773A>C
|
|
|
|
ENST00000647152.1:c.-290A>C
|
ENSP00000495893.1:n.-290A>C
|
|
|
ENST00000647209.1:c.*309A>C
|
ENSP00000495558.1:n.*309A>C
|
|
|
ENST00000647346.1:n.1460A>C
|
|
|
|
ENST00000299427.10:c.440A>C
|
ENSP00000299427.6:p.Glu147Ala
|
|
|
ENST00000428886.6:n.462A>C
|
|
|
|
ENST00000436873.6:c.440A>C
|
ENSP00000398136.2:p.Glu147Ala
|
|
|
ENST00000528571.5:c.*180A>C
|
ENSP00000434647.1:n.*180A>C
|
|
|
ENST00000533371.5:c.-290A>C
|
ENSP00000437066.1:n.-290A>C
|
|
|
ENST00000534644.5:n.425A>C
|
|
|
|
ENST00000611494.4:c.440A>C
|
ENSP00000484546.1:p.Glu147Ala
|
|
|
NM_000391.3:c.440A>C
|
NP_000382.3:p.Glu147Ala
|
|
|
NM_000391.4:c.440A>C
MANE Select
|
NP_000382.3:p.Glu147Ala
|
|
