ENST00000323130.8:c.1320G>C
|
ENSP00000314488.4:p.Arg440=
|
|
ENST00000409623.8:c.1289-14G>C
|
ENSP00000386966.4:n.1289-14G>C
|
|
ENST00000452276.6:c.1320G>C
|
ENSP00000388671.2:p.Arg440=
|
|
ENST00000453906.6:c.438G>C
|
ENSP00000403035.2:p.Arg146=
|
|
ENST00000520680.2:c.1320G>C
|
ENSP00000428785.2:p.Arg440=
|
|
ENST00000521517.6:c.1320G>C
|
ENSP00000430740.2:p.Arg440=
|
|
ENST00000681998.1:c.1141G>C
|
ENSP00000506773.1:n.1141G>C
|
|
ENST00000682036.1:c.438G>C
|
ENSP00000508390.1:p.Arg146=
|
|
ENST00000682577.1:c.1093G>C
|
ENSP00000506963.1:n.1093G>C
|
|
ENST00000682624.1:c.*894G>C
|
ENSP00000508343.1:n.*894G>C
|
|
ENST00000682700.1:c.1320G>C
|
ENSP00000507627.1:p.Arg440=
|
|
ENST00000682744.1:n.858G>C
|
|
|
ENST00000682804.1:n.1143G>C
|
|
|
ENST00000682837.1:c.809G>C
|
ENSP00000507920.1:n.809G>C
|
|
ENST00000682935.1:n.3370G>C
|
|
|
ENST00000682984.1:c.981G>C
|
ENSP00000507209.1:p.Arg327=
|
|
ENST00000683078.1:c.1075G>C
|
ENSP00000506796.1:n.1075G>C
|
|
ENST00000683223.1:c.1052G>C
|
ENSP00000507685.1:n.1052G>C
|
|
ENST00000683238.1:n.2544G>C
|
|
|
ENST00000683249.1:n.2917G>C
|
|
|
ENST00000683336.1:c.1141G>C
|
ENSP00000507695.1:n.1141G>C
|
|
ENST00000683362.1:c.981G>C
|
ENSP00000506985.1:p.Arg327=
|
|
ENST00000683850.1:n.1243G>C
|
|
|
ENST00000683919.1:c.1250G>C
|
ENSP00000507617.1:n.1250G>C
|
|
ENST00000683953.1:c.1231G>C
|
ENSP00000508375.1:n.1231G>C
|
|
ENST00000684023.1:c.1297G>C
|
ENSP00000507461.1:n.1297G>C
|
|
ENST00000684064.1:c.1011G>C
|
ENSP00000508192.1:p.Arg337=
|
|
ENST00000684089.1:n.2870G>C
|
|
|
ENST00000684149.1:c.*499G>C
|
ENSP00000507943.1:n.*499G>C
|
|
ENST00000684416.1:n.1279G>C
|
|
|
ENST00000684540.1:c.1250G>C
|
ENSP00000507987.1:n.1250G>C
|
|
ENST00000453321.8:c.1320G>C
MANE Select
|
ENSP00000389998.3:p.Arg440=
|
|
ENST00000323130.7:c.1290G>C
|
ENSP00000314488.3:p.Arg430=
|
|
ENST00000409623.7:c.1077G>C
|
ENSP00000386966.3:p.Arg359=
|
|
ENST00000452276.5:c.1011G>C
|
ENSP00000388671.1:p.Arg337=
|
|
ENST00000453321.7:c.1320G>C
|
ENSP00000389998.3:p.Arg440=
|
|
ENST00000453906.5:c.438G>C
|
ENSP00000403035.1:p.Arg146=
|
|
ENST00000474944.5:n.458G>C
|
|
|
ENST00000520680.1:c.142G>C
|
|
|
NM_001142301.1:c.1077G>C , LRG_688t2:c.1077G>C
|
NP_001135773.1:p.Arg359=
|
|
NM_153704.5:c.1320G>C , LRG_688t1:c.1320G>C
|
NP_714915.3:p.Arg440=
|
|
NR_024522.1:n.1391G>C
|
|
|
XM_006716686.2:c.1017G>C
|
XP_006716749.1:p.Arg339=
|
|
XM_006716687.2:c.720G>C
|
XP_006716750.1:p.Arg240=
|
|
XM_011517363.1:c.438G>C
|
XP_011515665.1:p.Arg146=
|
|
XR_428387.1:n.1378G>C
|
|
|
XR_928360.1:n.1378G>C
|
|
|
XR_928361.1:n.1378G>C
|
|
|
XR_928362.1:n.1378G>C
|
|
|
XM_006716686.4:c.1017G>C
|
XP_006716749.1:p.Arg339=
|
|
XM_011517363.3:c.438G>C
|
XP_011515665.1:p.Arg146=
|
|
XM_024447326.1:c.666G>C
|
XP_024303094.1:p.Arg222=
|
|
XR_001745619.2:n.1361G>C
|
|
|
XR_428387.2:n.1361G>C
|
|
|
XR_928360.3:n.1361G>C
|
|
|
XR_928362.3:n.1361G>C
|
|
|
NM_153704.6:c.1320G>C
MANE Select
|
NP_714915.3:p.Arg440=
|
|
NR_024522.2:n.1341G>C
|
|
|