|
NM_020937.4:c.4860A>G
MANE Select
|
NP_065988.1:p.Glu1620=
|
|
ENST00000267430.10:c.4860A>G
MANE Select
|
ENSP00000267430.5:p.Glu1620=
|
|
NM_001308133.1:c.4782A>G
|
NP_001295062.1:p.Glu1594=
|
|
NM_001308133.2:c.4782A>G
|
NP_001295062.1:p.Glu1594=
|
|
NM_020937.2:c.4860A>G , LRG_502t1:c.4860A>G
|
NP_065988.1:p.Glu1620=
|
|
NM_020937.3:c.4860A>G
|
NP_065988.1:p.Glu1620=
|
|
ENST00000267430.9:c.4860A>G
|
ENSP00000267430.5:p.Glu1620=
|
|
ENST00000542564.6:c.4782A>G
|
ENSP00000442493.2:p.Glu1594=
|
|
ENST00000554809.5:c.1657A>G
|
|
|
ENST00000554809.6:c.3072A>G
|
ENSP00000450632.2:p.Glu1024=
|
|
ENST00000555484.2:c.638A>G
|
|
|
ENST00000556250.5:c.3408A>G
|
ENSP00000452033.1:p.Glu1136=
|
|
ENST00000556250.6:c.4653A>G
|
ENSP00000452033.2:p.Glu1551=
|
|
ENST00000557110.2:c.638A>G
|
|
|
ENST00000696642.1:c.*3671A>G
|
ENSP00000512775.1:n.*3671A>G
|
|
ENST00000696645.1:n.750A>G
|
|
|
ENST00000696647.1:c.4860A>G
|
ENSP00000512778.1:p.Glu1620=
|
|
ENST00000696648.1:c.*2885A>G
|
ENSP00000512779.1:n.*2885A>G
|
|
ENST00000696649.1:c.4704A>G
|
ENSP00000512780.1:p.Glu1568=
|
|
ENST00000696650.1:n.4808A>G
|
|
|
ENST00000696659.1:c.2858A>G
|
|
|
ENST00000696663.1:c.3791A>G
|
|
|
ENST00000696664.1:c.3692A>G
|
|
|
ENST00000696665.1:c.638A>G
|
|
|
ENST00000696675.1:c.*616A>G
|
ENSP00000512799.1:n.*616A>G
|
|
ENST00000696683.1:c.3677A>G
|
|
|
ENST00000696684.1:c.3677A>G
|
|
|
ENST00000696685.1:c.3677A>G
|
|
|
ENST00000696686.1:n.1597A>G
|
|
|
XM_011537034.1:c.4875A>G
|
XP_011535336.1:p.Glu1625=
|
|
XM_011537034.2:c.4875A>G
|
XP_011535336.1:p.Glu1625=
|
|
XM_011537035.1:c.4797A>G
|
XP_011535337.1:p.Glu1599=
|
|
XM_011537035.3:c.4797A>G
|
XP_011535337.1:p.Glu1599=
|
|
XM_011537036.1:c.4875A>G
|
XP_011535338.1:p.Glu1625=
|
|
XM_011537037.1:c.2889A>G
|
XP_011535339.1:p.Glu963=
|
|
XM_011537037.3:c.2889A>G
|
XP_011535339.1:p.Glu963=
|
|
XM_017021523.1:c.4875A>G
|
XP_016877012.1:p.Glu1625=
|
|
XM_017021524.2:c.3912A>G
|
XP_016877013.1:p.Glu1304=
|
|
XM_017021525.2:c.3690A>G
|
XP_016877014.1:p.Glu1230=
|
|
XM_017021526.2:c.3690A>G
|
XP_016877015.1:p.Glu1230=
|
|
XM_017021527.1:c.3675A>G
|
XP_016877016.1:p.Glu1225=
|
|
XR_001750470.1:n.4967A>G
|
|
|
XR_001750471.2:n.4952A>G
|
|
|
XR_001750472.1:n.5004A>G
|
|