|
ENST00000323130.8:c.809T>G
|
ENSP00000314488.4:p.Leu270Arg
|
|
|
ENST00000409623.8:c.809T>G
|
ENSP00000386966.4:p.Leu270Arg
|
|
|
ENST00000452276.6:c.809T>G
|
ENSP00000388671.2:p.Leu270Arg
|
|
|
ENST00000453906.6:c.407-5536T>G
|
ENSP00000403035.2:n.407-5536T>G
|
|
|
ENST00000520680.2:c.809T>G
|
ENSP00000428785.2:p.Leu270Arg
|
|
|
ENST00000521065.2:c.*526T>G
|
ENSP00000427947.2:n.*526T>G
|
|
|
ENST00000521517.6:c.809T>G
|
ENSP00000430740.2:p.Leu270Arg
|
|
|
ENST00000681998.1:c.739T>G
|
ENSP00000506773.1:n.739T>G
|
|
|
ENST00000682036.1:c.407-5536T>G
|
ENSP00000508390.1:n.407-5536T>G
|
|
|
ENST00000682577.1:c.739T>G
|
ENSP00000506963.1:n.739T>G
|
|
|
ENST00000682624.1:c.*383T>G
|
ENSP00000508343.1:n.*383T>G
|
|
|
ENST00000682700.1:c.809T>G
|
ENSP00000507627.1:p.Leu270Arg
|
|
|
ENST00000682744.1:n.347T>G
|
|
|
|
ENST00000682804.1:n.632T>G
|
|
|
|
ENST00000682837.1:c.564T>G
|
ENSP00000507920.1:n.564T>G
|
|
|
ENST00000682935.1:n.2369T>G
|
|
|
|
ENST00000682984.1:c.470T>G
|
ENSP00000507209.1:p.Leu157Arg
|
|
|
ENST00000683078.1:c.564T>G
|
ENSP00000506796.1:n.564T>G
|
|
|
ENST00000683223.1:c.650T>G
|
ENSP00000507685.1:n.650T>G
|
|
|
ENST00000683238.1:n.2190T>G
|
|
|
|
ENST00000683249.1:n.2390T>G
|
|
|
|
ENST00000683336.1:c.739T>G
|
ENSP00000507695.1:n.739T>G
|
|
|
ENST00000683362.1:c.470T>G
|
ENSP00000506985.1:p.Leu157Arg
|
|
|
ENST00000683850.1:n.732T>G
|
|
|
|
ENST00000683919.1:c.739T>G
|
ENSP00000507617.1:n.739T>G
|
|
|
ENST00000683953.1:c.720T>G
|
ENSP00000508375.1:n.720T>G
|
|
|
ENST00000684023.1:c.943T>G
|
ENSP00000507461.1:n.943T>G
|
|
|
ENST00000684064.1:c.500T>G
|
ENSP00000508192.1:p.Leu167Arg
|
|
|
ENST00000684089.1:n.2359T>G
|
|
|
|
ENST00000684149.1:c.*145T>G
|
ENSP00000507943.1:n.*145T>G
|
|
|
ENST00000684416.1:n.768T>G
|
|
|
|
ENST00000684540.1:c.739T>G
|
ENSP00000507987.1:n.739T>G
|
|
|
ENST00000453321.8:c.809T>G
MANE Select
|
ENSP00000389998.3:p.Leu270Arg
|
|
|
ENST00000323130.7:c.779T>G
|
ENSP00000314488.3:p.Leu260Arg
|
|
|
ENST00000409623.7:c.566T>G
|
ENSP00000386966.3:p.Leu189Arg
|
|
|
ENST00000425545.2:n.256T>G
|
|
|
|
ENST00000452276.5:c.500T>G
|
ENSP00000388671.1:p.Leu167Arg
|
|
|
ENST00000453321.7:c.809T>G
|
ENSP00000389998.3:p.Leu270Arg
|
|
|
ENST00000453906.5:c.407-5536T>G
|
ENSP00000403035.1:n.407-5536T>G
|
|
|
ENST00000474944.5:n.427-5536T>G
|
|
|
|
ENST00000496213.5:n.274T>G
|
|
|
|
NM_001142301.1:c.566T>G , LRG_688t2:c.566T>G
|
NP_001135773.1:p.Leu189Arg
|
|
|
NM_153704.5:c.809T>G , LRG_688t1:c.809T>G
|
NP_714915.3:p.Leu270Arg
|
|
|
NR_024522.1:n.880T>G
|
|
|
|
XM_006716686.2:c.506T>G
|
XP_006716749.1:p.Leu169Arg
|
|
|
XM_006716687.2:c.209T>G
|
XP_006716750.1:p.Leu70Arg
|
|
|
XM_011517363.1:c.407-5536T>G
|
XP_011515665.1:n.407-5536T>G
|
|
|
XR_428387.1:n.867T>G
|
|
|
|
XR_928360.1:n.867T>G
|
|
|
|
XR_928361.1:n.867T>G
|
|
|
|
XR_928362.1:n.867T>G
|
|
|
|
XM_006716686.4:c.506T>G
|
XP_006716749.1:p.Leu169Arg
|
|
|
XM_011517363.3:c.407-5536T>G
|
XP_011515665.1:n.407-5536T>G
|
|
|
XM_024447326.1:c.155T>G
|
XP_024303094.1:p.Leu52Arg
|
|
|
XR_001745619.2:n.850T>G
|
|
|
|
XR_428387.2:n.850T>G
|
|
|
|
XR_928360.3:n.850T>G
|
|
|
|
XR_928362.3:n.850T>G
|
|
|
|
NM_153704.6:c.809T>G
MANE Select
|
NP_714915.3:p.Leu270Arg
|
|
|
NR_024522.2:n.830T>G
|
|
|
