ENST00000554809.6:c.2848T>C
|
ENSP00000450632.2:p.Leu950=
|
|
ENST00000555484.2:c.414T>C
|
|
|
ENST00000556250.6:c.4429T>C
|
ENSP00000452033.2:p.Leu1477=
|
|
ENST00000557110.2:c.414T>C
|
|
|
ENST00000696642.1:c.*3447T>C
|
ENSP00000512775.1:n.*3447T>C
|
|
ENST00000696644.1:n.372T>C
|
|
|
ENST00000696645.1:n.526T>C
|
|
|
ENST00000696647.1:c.4636T>C
|
ENSP00000512778.1:p.Leu1546=
|
|
ENST00000696648.1:c.*2661T>C
|
ENSP00000512779.1:n.*2661T>C
|
|
ENST00000696649.1:c.4480T>C
|
ENSP00000512780.1:p.Leu1494=
|
|
ENST00000696650.1:n.4584T>C
|
|
|
ENST00000696659.1:c.2634T>C
|
|
|
ENST00000696663.1:c.3567T>C
|
|
|
ENST00000696664.1:c.3468T>C
|
|
|
ENST00000696665.1:c.414T>C
|
|
|
ENST00000696675.1:c.*392T>C
|
ENSP00000512799.1:n.*392T>C
|
|
ENST00000696683.1:c.3453T>C
|
|
|
ENST00000696684.1:c.3453T>C
|
|
|
ENST00000696685.1:c.3453T>C
|
|
|
ENST00000696686.1:n.1373T>C
|
|
|
ENST00000267430.10:c.4636T>C
MANE Select
|
ENSP00000267430.5:p.Leu1546=
|
|
ENST00000267430.9:c.4636T>C
|
ENSP00000267430.5:p.Leu1546=
|
|
ENST00000542564.6:c.4558T>C
|
ENSP00000442493.2:p.Leu1520=
|
|
ENST00000554809.5:c.1433T>C
|
|
|
ENST00000555013.1:n.469T>C
|
|
|
ENST00000556250.5:c.3184T>C
|
ENSP00000452033.1:p.Leu1062=
|
|
NM_001308133.1:c.4558T>C
|
NP_001295062.1:p.Leu1520=
|
|
NM_020937.2:c.4636T>C , LRG_502t1:c.4636T>C
|
NP_065988.1:p.Leu1546=
|
|
NM_020937.3:c.4636T>C
|
NP_065988.1:p.Leu1546=
|
|
XM_011537034.1:c.4651T>C
|
XP_011535336.1:p.Leu1551=
|
|
XM_011537035.1:c.4573T>C
|
XP_011535337.1:p.Leu1525=
|
|
XM_011537036.1:c.4651T>C
|
XP_011535338.1:p.Leu1551=
|
|
XM_011537037.1:c.2665T>C
|
XP_011535339.1:p.Leu889=
|
|
XM_011537034.2:c.4651T>C
|
XP_011535336.1:p.Leu1551=
|
|
XM_011537035.3:c.4573T>C
|
XP_011535337.1:p.Leu1525=
|
|
XM_011537037.3:c.2665T>C
|
XP_011535339.1:p.Leu889=
|
|
XM_017021523.1:c.4651T>C
|
XP_016877012.1:p.Leu1551=
|
|
XM_017021524.2:c.3688T>C
|
XP_016877013.1:p.Leu1230=
|
|
XM_017021525.2:c.3466T>C
|
XP_016877014.1:p.Leu1156=
|
|
XM_017021526.2:c.3466T>C
|
XP_016877015.1:p.Leu1156=
|
|
XM_017021527.1:c.3451T>C
|
XP_016877016.1:p.Leu1151=
|
|
XR_001750470.1:n.4743T>C
|
|
|
XR_001750471.2:n.4728T>C
|
|
|
XR_001750472.1:n.4780T>C
|
|
|
NM_020937.4:c.4636T>C
MANE Select
|
NP_065988.1:p.Leu1546=
|
|
NM_001308133.2:c.4558T>C
|
NP_001295062.1:p.Leu1520=
|
|