ENST00000554809.6:c.2841T>A
|
ENSP00000450632.2:p.Leu947=
|
|
ENST00000555484.2:c.407T>A
|
|
|
ENST00000556250.6:c.4422T>A
|
ENSP00000452033.2:p.Leu1474=
|
|
ENST00000557110.2:c.407T>A
|
|
|
ENST00000696642.1:c.*3440T>A
|
ENSP00000512775.1:n.*3440T>A
|
|
ENST00000696644.1:n.365T>A
|
|
|
ENST00000696645.1:n.519T>A
|
|
|
ENST00000696647.1:c.4629T>A
|
ENSP00000512778.1:p.Leu1543=
|
|
ENST00000696648.1:c.*2654T>A
|
ENSP00000512779.1:n.*2654T>A
|
|
ENST00000696649.1:c.4473T>A
|
ENSP00000512780.1:p.Leu1491=
|
|
ENST00000696650.1:n.4577T>A
|
|
|
ENST00000696659.1:c.2627T>A
|
|
|
ENST00000696663.1:c.3560T>A
|
|
|
ENST00000696664.1:c.3461T>A
|
|
|
ENST00000696665.1:c.407T>A
|
|
|
ENST00000696675.1:c.*385T>A
|
ENSP00000512799.1:n.*385T>A
|
|
ENST00000696683.1:c.3446T>A
|
|
|
ENST00000696684.1:c.3446T>A
|
|
|
ENST00000696685.1:c.3446T>A
|
|
|
ENST00000696686.1:n.1366T>A
|
|
|
ENST00000267430.10:c.4629T>A
MANE Select
|
ENSP00000267430.5:p.Leu1543=
|
|
ENST00000267430.9:c.4629T>A
|
ENSP00000267430.5:p.Leu1543=
|
|
ENST00000542564.6:c.4551T>A
|
ENSP00000442493.2:p.Leu1517=
|
|
ENST00000554809.5:c.1426T>A
|
|
|
ENST00000555013.1:n.462T>A
|
|
|
ENST00000556250.5:c.3177T>A
|
ENSP00000452033.1:p.Leu1059=
|
|
NM_001308133.1:c.4551T>A
|
NP_001295062.1:p.Leu1517=
|
|
NM_020937.2:c.4629T>A , LRG_502t1:c.4629T>A
|
NP_065988.1:p.Leu1543=
|
|
NM_020937.3:c.4629T>A
|
NP_065988.1:p.Leu1543=
|
|
XM_011537034.1:c.4644T>A
|
XP_011535336.1:p.Leu1548=
|
|
XM_011537035.1:c.4566T>A
|
XP_011535337.1:p.Leu1522=
|
|
XM_011537036.1:c.4644T>A
|
XP_011535338.1:p.Leu1548=
|
|
XM_011537037.1:c.2658T>A
|
XP_011535339.1:p.Leu886=
|
|
XM_011537034.2:c.4644T>A
|
XP_011535336.1:p.Leu1548=
|
|
XM_011537035.3:c.4566T>A
|
XP_011535337.1:p.Leu1522=
|
|
XM_011537037.3:c.2658T>A
|
XP_011535339.1:p.Leu886=
|
|
XM_017021523.1:c.4644T>A
|
XP_016877012.1:p.Leu1548=
|
|
XM_017021524.2:c.3681T>A
|
XP_016877013.1:p.Leu1227=
|
|
XM_017021525.2:c.3459T>A
|
XP_016877014.1:p.Leu1153=
|
|
XM_017021526.2:c.3459T>A
|
XP_016877015.1:p.Leu1153=
|
|
XM_017021527.1:c.3444T>A
|
XP_016877016.1:p.Leu1148=
|
|
XR_001750470.1:n.4736T>A
|
|
|
XR_001750471.2:n.4721T>A
|
|
|
XR_001750472.1:n.4773T>A
|
|
|
NM_020937.4:c.4629T>A
MANE Select
|
NP_065988.1:p.Leu1543=
|
|
NM_001308133.2:c.4551T>A
|
NP_001295062.1:p.Leu1517=
|
|