ENST00000554809.6:c.2838A>G
|
ENSP00000450632.2:p.Leu946=
|
|
ENST00000555484.2:c.404A>G
|
|
|
ENST00000556250.6:c.4419A>G
|
ENSP00000452033.2:p.Leu1473=
|
|
ENST00000557110.2:c.404A>G
|
|
|
ENST00000696642.1:c.*3437A>G
|
ENSP00000512775.1:n.*3437A>G
|
|
ENST00000696644.1:n.362A>G
|
|
|
ENST00000696645.1:n.516A>G
|
|
|
ENST00000696647.1:c.4626A>G
|
ENSP00000512778.1:p.Leu1542=
|
|
ENST00000696648.1:c.*2651A>G
|
ENSP00000512779.1:n.*2651A>G
|
|
ENST00000696649.1:c.4470A>G
|
ENSP00000512780.1:p.Leu1490=
|
|
ENST00000696650.1:n.4574A>G
|
|
|
ENST00000696659.1:c.2624A>G
|
|
|
ENST00000696663.1:c.3557A>G
|
|
|
ENST00000696664.1:c.3458A>G
|
|
|
ENST00000696665.1:c.404A>G
|
|
|
ENST00000696675.1:c.*382A>G
|
ENSP00000512799.1:n.*382A>G
|
|
ENST00000696683.1:c.3443A>G
|
|
|
ENST00000696684.1:c.3443A>G
|
|
|
ENST00000696685.1:c.3443A>G
|
|
|
ENST00000696686.1:n.1363A>G
|
|
|
ENST00000267430.10:c.4626A>G
MANE Select
|
ENSP00000267430.5:p.Leu1542=
|
|
ENST00000267430.9:c.4626A>G
|
ENSP00000267430.5:p.Leu1542=
|
|
ENST00000542564.6:c.4548A>G
|
ENSP00000442493.2:p.Leu1516=
|
|
ENST00000554809.5:c.1423A>G
|
|
|
ENST00000555013.1:n.459A>G
|
|
|
ENST00000556250.5:c.3174A>G
|
ENSP00000452033.1:p.Leu1058=
|
|
NM_001308133.1:c.4548A>G
|
NP_001295062.1:p.Leu1516=
|
|
NM_020937.2:c.4626A>G , LRG_502t1:c.4626A>G
|
NP_065988.1:p.Leu1542=
|
|
NM_020937.3:c.4626A>G
|
NP_065988.1:p.Leu1542=
|
|
XM_011537034.1:c.4641A>G
|
XP_011535336.1:p.Leu1547=
|
|
XM_011537035.1:c.4563A>G
|
XP_011535337.1:p.Leu1521=
|
|
XM_011537036.1:c.4641A>G
|
XP_011535338.1:p.Leu1547=
|
|
XM_011537037.1:c.2655A>G
|
XP_011535339.1:p.Leu885=
|
|
XM_011537034.2:c.4641A>G
|
XP_011535336.1:p.Leu1547=
|
|
XM_011537035.3:c.4563A>G
|
XP_011535337.1:p.Leu1521=
|
|
XM_011537037.3:c.2655A>G
|
XP_011535339.1:p.Leu885=
|
|
XM_017021523.1:c.4641A>G
|
XP_016877012.1:p.Leu1547=
|
|
XM_017021524.2:c.3678A>G
|
XP_016877013.1:p.Leu1226=
|
|
XM_017021525.2:c.3456A>G
|
XP_016877014.1:p.Leu1152=
|
|
XM_017021526.2:c.3456A>G
|
XP_016877015.1:p.Leu1152=
|
|
XM_017021527.1:c.3441A>G
|
XP_016877016.1:p.Leu1147=
|
|
XR_001750470.1:n.4733A>G
|
|
|
XR_001750471.2:n.4718A>G
|
|
|
XR_001750472.1:n.4770A>G
|
|
|
NM_020937.4:c.4626A>G
MANE Select
|
NP_065988.1:p.Leu1542=
|
|
NM_001308133.2:c.4548A>G
|
NP_001295062.1:p.Leu1516=
|
|