ENST00000554809.6:c.2772A=
|
ENSP00000450632.2:p.Glu924=
|
|
ENST00000555484.2:c.338A=
|
|
|
ENST00000556250.6:c.4353A=
|
ENSP00000452033.2:p.Glu1451=
|
|
ENST00000557110.2:c.338A=
|
|
|
ENST00000696642.1:c.*3371A=
|
ENSP00000512775.1:n.*3371A=
|
|
ENST00000696644.1:n.296A=
|
|
|
ENST00000696645.1:n.450A=
|
|
|
ENST00000696647.1:c.4560A=
|
ENSP00000512778.1:p.Glu1520=
|
|
ENST00000696648.1:c.*2585A=
|
ENSP00000512779.1:n.*2585A=
|
|
ENST00000696649.1:c.4404A=
|
ENSP00000512780.1:p.Glu1468=
|
|
ENST00000696650.1:n.4508A=
|
|
|
ENST00000696659.1:c.2558A=
|
|
|
ENST00000696663.1:c.3491A=
|
|
|
ENST00000696664.1:c.3392A=
|
|
|
ENST00000696665.1:c.338A=
|
|
|
ENST00000696675.1:c.*316A=
|
ENSP00000512799.1:n.*316A=
|
|
ENST00000696683.1:c.3377A=
|
|
|
ENST00000696684.1:c.3377A=
|
|
|
ENST00000696685.1:c.3377A=
|
|
|
ENST00000696686.1:n.1297A=
|
|
|
ENST00000267430.10:c.4560A=
MANE Select
|
ENSP00000267430.5:p.Glu1520=
|
|
ENST00000267430.9:c.4560A=
|
ENSP00000267430.5:p.Glu1520=
|
|
ENST00000542564.6:c.4482A=
|
ENSP00000442493.2:p.Glu1494=
|
|
ENST00000554809.5:c.1357A=
|
|
|
ENST00000555013.1:n.393A=
|
|
|
ENST00000556250.5:c.3108A=
|
ENSP00000452033.1:p.Glu1036=
|
|
NM_001308133.1:c.4482A=
|
NP_001295062.1:p.Glu1494=
|
|
NM_020937.2:c.4560A= , LRG_502t1:c.4560A=
|
NP_065988.1:p.Glu1520=
|
|
NM_020937.3:c.4560A=
|
NP_065988.1:p.Glu1520=
|
|
XM_011537034.1:c.4575A=
|
XP_011535336.1:p.Glu1525=
|
|
XM_011537035.1:c.4497A=
|
XP_011535337.1:p.Glu1499=
|
|
XM_011537036.1:c.4575A=
|
XP_011535338.1:p.Glu1525=
|
|
XM_011537037.1:c.2589A=
|
XP_011535339.1:p.Glu863=
|
|
XM_011537034.2:c.4575A=
|
XP_011535336.1:p.Glu1525=
|
|
XM_011537035.3:c.4497A=
|
XP_011535337.1:p.Glu1499=
|
|
XM_011537037.3:c.2589A=
|
XP_011535339.1:p.Glu863=
|
|
XM_017021523.1:c.4575A=
|
XP_016877012.1:p.Glu1525=
|
|
XM_017021524.2:c.3612A=
|
XP_016877013.1:p.Glu1204=
|
|
XM_017021525.2:c.3390A=
|
XP_016877014.1:p.Glu1130=
|
|
XM_017021526.2:c.3390A=
|
XP_016877015.1:p.Glu1130=
|
|
XM_017021527.1:c.3375A=
|
XP_016877016.1:p.Glu1125=
|
|
XR_001750470.1:n.4667A=
|
|
|
XR_001750471.2:n.4652A=
|
|
|
XR_001750472.1:n.4704A=
|
|
|
NM_020937.4:c.4560A=
MANE Select
|
NP_065988.1:p.Glu1520=
|
|
NM_001308133.2:c.4482A=
|
NP_001295062.1:p.Glu1494=
|
|