ENST00000554809.6:c.2823A>G
|
ENSP00000450632.2:p.Glu941=
|
|
ENST00000555484.2:c.389A>G
|
|
|
ENST00000556250.6:c.4404A>G
|
ENSP00000452033.2:p.Glu1468=
|
|
ENST00000557110.2:c.389A>G
|
|
|
ENST00000696642.1:c.*3422A>G
|
ENSP00000512775.1:n.*3422A>G
|
|
ENST00000696644.1:n.347A>G
|
|
|
ENST00000696645.1:n.501A>G
|
|
|
ENST00000696647.1:c.4611A>G
|
ENSP00000512778.1:p.Glu1537=
|
|
ENST00000696648.1:c.*2636A>G
|
ENSP00000512779.1:n.*2636A>G
|
|
ENST00000696649.1:c.4455A>G
|
ENSP00000512780.1:p.Glu1485=
|
|
ENST00000696650.1:n.4559A>G
|
|
|
ENST00000696659.1:c.2609A>G
|
|
|
ENST00000696663.1:c.3542A>G
|
|
|
ENST00000696664.1:c.3443A>G
|
|
|
ENST00000696665.1:c.389A>G
|
|
|
ENST00000696675.1:c.*367A>G
|
ENSP00000512799.1:n.*367A>G
|
|
ENST00000696683.1:c.3428A>G
|
|
|
ENST00000696684.1:c.3428A>G
|
|
|
ENST00000696685.1:c.3428A>G
|
|
|
ENST00000696686.1:n.1348A>G
|
|
|
ENST00000267430.10:c.4611A>G
MANE Select
|
ENSP00000267430.5:p.Glu1537=
|
|
ENST00000267430.9:c.4611A>G
|
ENSP00000267430.5:p.Glu1537=
|
|
ENST00000542564.6:c.4533A>G
|
ENSP00000442493.2:p.Glu1511=
|
|
ENST00000554809.5:c.1408A>G
|
|
|
ENST00000555013.1:n.444A>G
|
|
|
ENST00000556250.5:c.3159A>G
|
ENSP00000452033.1:p.Glu1053=
|
|
NM_001308133.1:c.4533A>G
|
NP_001295062.1:p.Glu1511=
|
|
NM_020937.2:c.4611A>G , LRG_502t1:c.4611A>G
|
NP_065988.1:p.Glu1537=
|
|
NM_020937.3:c.4611A>G
|
NP_065988.1:p.Glu1537=
|
|
XM_011537034.1:c.4626A>G
|
XP_011535336.1:p.Glu1542=
|
|
XM_011537035.1:c.4548A>G
|
XP_011535337.1:p.Glu1516=
|
|
XM_011537036.1:c.4626A>G
|
XP_011535338.1:p.Glu1542=
|
|
XM_011537037.1:c.2640A>G
|
XP_011535339.1:p.Glu880=
|
|
XM_011537034.2:c.4626A>G
|
XP_011535336.1:p.Glu1542=
|
|
XM_011537035.3:c.4548A>G
|
XP_011535337.1:p.Glu1516=
|
|
XM_011537037.3:c.2640A>G
|
XP_011535339.1:p.Glu880=
|
|
XM_017021523.1:c.4626A>G
|
XP_016877012.1:p.Glu1542=
|
|
XM_017021524.2:c.3663A>G
|
XP_016877013.1:p.Glu1221=
|
|
XM_017021525.2:c.3441A>G
|
XP_016877014.1:p.Glu1147=
|
|
XM_017021526.2:c.3441A>G
|
XP_016877015.1:p.Glu1147=
|
|
XM_017021527.1:c.3426A>G
|
XP_016877016.1:p.Glu1142=
|
|
XR_001750470.1:n.4718A>G
|
|
|
XR_001750471.2:n.4703A>G
|
|
|
XR_001750472.1:n.4755A>G
|
|
|
NM_020937.4:c.4611A>G
MANE Select
|
NP_065988.1:p.Glu1537=
|
|
NM_001308133.2:c.4533A>G
|
NP_001295062.1:p.Glu1511=
|
|