ENST00000554809.6:c.2799T>A
|
ENSP00000450632.2:p.Asp933Glu
|
|
ENST00000555484.2:c.365T>A
|
|
|
ENST00000556250.6:c.4380T>A
|
ENSP00000452033.2:p.Asp1460Glu
|
|
ENST00000557110.2:c.365T>A
|
|
|
ENST00000696642.1:c.*3398T>A
|
ENSP00000512775.1:n.*3398T>A
|
|
ENST00000696644.1:n.323T>A
|
|
|
ENST00000696645.1:n.477T>A
|
|
|
ENST00000696647.1:c.4587T>A
|
ENSP00000512778.1:p.Asp1529Glu
|
|
ENST00000696648.1:c.*2612T>A
|
ENSP00000512779.1:n.*2612T>A
|
|
ENST00000696649.1:c.4431T>A
|
ENSP00000512780.1:p.Asp1477Glu
|
|
ENST00000696650.1:n.4535T>A
|
|
|
ENST00000696659.1:c.2585T>A
|
|
|
ENST00000696663.1:c.3518T>A
|
|
|
ENST00000696664.1:c.3419T>A
|
|
|
ENST00000696665.1:c.365T>A
|
|
|
ENST00000696675.1:c.*343T>A
|
ENSP00000512799.1:n.*343T>A
|
|
ENST00000696683.1:c.3404T>A
|
|
|
ENST00000696684.1:c.3404T>A
|
|
|
ENST00000696685.1:c.3404T>A
|
|
|
ENST00000696686.1:n.1324T>A
|
|
|
ENST00000267430.10:c.4587T>A
MANE Select
|
ENSP00000267430.5:p.Asp1529Glu
|
|
ENST00000267430.9:c.4587T>A
|
ENSP00000267430.5:p.Asp1529Glu
|
|
ENST00000542564.6:c.4509T>A
|
ENSP00000442493.2:p.Asp1503Glu
|
|
ENST00000554809.5:c.1384T>A
|
|
|
ENST00000555013.1:n.420T>A
|
|
|
ENST00000556250.5:c.3135T>A
|
ENSP00000452033.1:p.Asp1045Glu
|
|
NM_001308133.1:c.4509T>A
|
NP_001295062.1:p.Asp1503Glu
|
|
NM_020937.2:c.4587T>A , LRG_502t1:c.4587T>A
|
NP_065988.1:p.Asp1529Glu
|
|
NM_020937.3:c.4587T>A
|
NP_065988.1:p.Asp1529Glu
|
|
XM_011537034.1:c.4602T>A
|
XP_011535336.1:p.Asp1534Glu
|
|
XM_011537035.1:c.4524T>A
|
XP_011535337.1:p.Asp1508Glu
|
|
XM_011537036.1:c.4602T>A
|
XP_011535338.1:p.Asp1534Glu
|
|
XM_011537037.1:c.2616T>A
|
XP_011535339.1:p.Asp872Glu
|
|
XM_011537034.2:c.4602T>A
|
XP_011535336.1:p.Asp1534Glu
|
|
XM_011537035.3:c.4524T>A
|
XP_011535337.1:p.Asp1508Glu
|
|
XM_011537037.3:c.2616T>A
|
XP_011535339.1:p.Asp872Glu
|
|
XM_017021523.1:c.4602T>A
|
XP_016877012.1:p.Asp1534Glu
|
|
XM_017021524.2:c.3639T>A
|
XP_016877013.1:p.Asp1213Glu
|
|
XM_017021525.2:c.3417T>A
|
XP_016877014.1:p.Asp1139Glu
|
|
XM_017021526.2:c.3417T>A
|
XP_016877015.1:p.Asp1139Glu
|
|
XM_017021527.1:c.3402T>A
|
XP_016877016.1:p.Asp1134Glu
|
|
XR_001750470.1:n.4694T>A
|
|
|
XR_001750471.2:n.4679T>A
|
|
|
XR_001750472.1:n.4731T>A
|
|
|
NM_020937.4:c.4587T>A
MANE Select
|
NP_065988.1:p.Asp1529Glu
|
|
NM_001308133.2:c.4509T>A
|
NP_001295062.1:p.Asp1503Glu
|
|