ENST00000554809.6:c.2817A>T
|
ENSP00000450632.2:p.Glu939Asp
|
|
ENST00000555484.2:c.383A>T
|
|
|
ENST00000556250.6:c.4398A>T
|
ENSP00000452033.2:p.Glu1466Asp
|
|
ENST00000557110.2:c.383A>T
|
|
|
ENST00000696642.1:c.*3416A>T
|
ENSP00000512775.1:n.*3416A>T
|
|
ENST00000696644.1:n.341A>T
|
|
|
ENST00000696645.1:n.495A>T
|
|
|
ENST00000696647.1:c.4605A>T
|
ENSP00000512778.1:p.Glu1535Asp
|
|
ENST00000696648.1:c.*2630A>T
|
ENSP00000512779.1:n.*2630A>T
|
|
ENST00000696649.1:c.4449A>T
|
ENSP00000512780.1:p.Glu1483Asp
|
|
ENST00000696650.1:n.4553A>T
|
|
|
ENST00000696659.1:c.2603A>T
|
|
|
ENST00000696663.1:c.3536A>T
|
|
|
ENST00000696664.1:c.3437A>T
|
|
|
ENST00000696665.1:c.383A>T
|
|
|
ENST00000696675.1:c.*361A>T
|
ENSP00000512799.1:n.*361A>T
|
|
ENST00000696683.1:c.3422A>T
|
|
|
ENST00000696684.1:c.3422A>T
|
|
|
ENST00000696685.1:c.3422A>T
|
|
|
ENST00000696686.1:n.1342A>T
|
|
|
ENST00000267430.10:c.4605A>T
MANE Select
|
ENSP00000267430.5:p.Glu1535Asp
|
|
ENST00000267430.9:c.4605A>T
|
ENSP00000267430.5:p.Glu1535Asp
|
|
ENST00000542564.6:c.4527A>T
|
ENSP00000442493.2:p.Glu1509Asp
|
|
ENST00000554809.5:c.1402A>T
|
|
|
ENST00000555013.1:n.438A>T
|
|
|
ENST00000556250.5:c.3153A>T
|
ENSP00000452033.1:p.Glu1051Asp
|
|
NM_001308133.1:c.4527A>T
|
NP_001295062.1:p.Glu1509Asp
|
|
NM_020937.2:c.4605A>T , LRG_502t1:c.4605A>T
|
NP_065988.1:p.Glu1535Asp
|
|
NM_020937.3:c.4605A>T
|
NP_065988.1:p.Glu1535Asp
|
|
XM_011537034.1:c.4620A>T
|
XP_011535336.1:p.Glu1540Asp
|
|
XM_011537035.1:c.4542A>T
|
XP_011535337.1:p.Glu1514Asp
|
|
XM_011537036.1:c.4620A>T
|
XP_011535338.1:p.Glu1540Asp
|
|
XM_011537037.1:c.2634A>T
|
XP_011535339.1:p.Glu878Asp
|
|
XM_011537034.2:c.4620A>T
|
XP_011535336.1:p.Glu1540Asp
|
|
XM_011537035.3:c.4542A>T
|
XP_011535337.1:p.Glu1514Asp
|
|
XM_011537037.3:c.2634A>T
|
XP_011535339.1:p.Glu878Asp
|
|
XM_017021523.1:c.4620A>T
|
XP_016877012.1:p.Glu1540Asp
|
|
XM_017021524.2:c.3657A>T
|
XP_016877013.1:p.Glu1219Asp
|
|
XM_017021525.2:c.3435A>T
|
XP_016877014.1:p.Glu1145Asp
|
|
XM_017021526.2:c.3435A>T
|
XP_016877015.1:p.Glu1145Asp
|
|
XM_017021527.1:c.3420A>T
|
XP_016877016.1:p.Glu1140Asp
|
|
XR_001750470.1:n.4712A>T
|
|
|
XR_001750471.2:n.4697A>T
|
|
|
XR_001750472.1:n.4749A>T
|
|
|
NM_020937.4:c.4605A>T
MANE Select
|
NP_065988.1:p.Glu1535Asp
|
|
NM_001308133.2:c.4527A>T
|
NP_001295062.1:p.Glu1509Asp
|
|