|
ENST00000323130.8:c.731C>G
|
ENSP00000314488.4:p.Thr244Arg
|
|
|
ENST00000409623.8:c.731C>G
|
ENSP00000386966.4:p.Thr244Arg
|
|
|
ENST00000452276.6:c.731C>G
|
ENSP00000388671.2:p.Thr244Arg
|
|
|
ENST00000453906.6:c.407-5614C>G
|
ENSP00000403035.2:n.407-5614C>G
|
|
|
ENST00000520680.2:c.731C>G
|
ENSP00000428785.2:p.Thr244Arg
|
|
|
ENST00000521065.2:c.*448C>G
|
ENSP00000427947.2:n.*448C>G
|
|
|
ENST00000521517.6:c.731C>G
|
ENSP00000430740.2:p.Thr244Arg
|
|
|
ENST00000681998.1:c.661C>G
|
ENSP00000506773.1:n.661C>G
|
|
|
ENST00000682036.1:c.407-5614C>G
|
ENSP00000508390.1:n.407-5614C>G
|
|
|
ENST00000682577.1:c.661C>G
|
ENSP00000506963.1:n.661C>G
|
|
|
ENST00000682624.1:c.*305C>G
|
ENSP00000508343.1:n.*305C>G
|
|
|
ENST00000682700.1:c.731C>G
|
ENSP00000507627.1:p.Thr244Arg
|
|
|
ENST00000682744.1:n.269C>G
|
|
|
|
ENST00000682804.1:n.554C>G
|
|
|
|
ENST00000682837.1:c.486C>G
|
ENSP00000507920.1:p.Asn162Lys
|
|
|
ENST00000682935.1:n.2291C>G
|
|
|
|
ENST00000682984.1:c.392C>G
|
ENSP00000507209.1:p.Thr131Arg
|
|
|
ENST00000683078.1:c.486C>G
|
ENSP00000506796.1:p.Asn162Lys
|
|
|
ENST00000683223.1:c.572C>G
|
ENSP00000507685.1:n.572C>G
|
|
|
ENST00000683238.1:n.2112C>G
|
|
|
|
ENST00000683249.1:n.2312C>G
|
|
|
|
ENST00000683336.1:c.661C>G
|
ENSP00000507695.1:n.661C>G
|
|
|
ENST00000683362.1:c.392C>G
|
ENSP00000506985.1:p.Thr131Arg
|
|
|
ENST00000683850.1:n.654C>G
|
|
|
|
ENST00000683919.1:c.661C>G
|
ENSP00000507617.1:n.661C>G
|
|
|
ENST00000683953.1:c.642C>G
|
ENSP00000508375.1:n.642C>G
|
|
|
ENST00000684023.1:c.865C>G
|
ENSP00000507461.1:n.865C>G
|
|
|
ENST00000684064.1:c.422C>G
|
ENSP00000508192.1:p.Thr141Arg
|
|
|
ENST00000684089.1:n.2281C>G
|
|
|
|
ENST00000684149.1:c.*67C>G
|
ENSP00000507943.1:n.*67C>G
|
|
|
ENST00000684416.1:n.690C>G
|
|
|
|
ENST00000684540.1:c.661C>G
|
ENSP00000507987.1:n.661C>G
|
|
|
ENST00000453321.8:c.731C>G
MANE Select
|
ENSP00000389998.3:p.Thr244Arg
|
|
|
ENST00000323130.7:c.701C>G
|
ENSP00000314488.3:p.Thr234Arg
|
|
|
ENST00000409623.7:c.488C>G
|
ENSP00000386966.3:p.Thr163Arg
|
|
|
ENST00000425545.2:n.178C>G
|
|
|
|
ENST00000452276.5:c.422C>G
|
ENSP00000388671.1:p.Thr141Arg
|
|
|
ENST00000453321.7:c.731C>G
|
ENSP00000389998.3:p.Thr244Arg
|
|
|
ENST00000453906.5:c.407-5614C>G
|
ENSP00000403035.1:n.407-5614C>G
|
|
|
ENST00000474944.5:n.427-5614C>G
|
|
|
|
ENST00000496213.5:n.196C>G
|
|
|
|
NM_001142301.1:c.488C>G , LRG_688t2:c.488C>G
|
NP_001135773.1:p.Thr163Arg
|
|
|
NM_153704.5:c.731C>G , LRG_688t1:c.731C>G
|
NP_714915.3:p.Thr244Arg
|
|
|
NR_024522.1:n.802C>G
|
|
|
|
XM_006716686.2:c.428C>G
|
XP_006716749.1:p.Thr143Arg
|
|
|
XM_006716687.2:c.131C>G
|
XP_006716750.1:p.Thr44Arg
|
|
|
XM_011517363.1:c.407-5614C>G
|
XP_011515665.1:n.407-5614C>G
|
|
|
XR_428387.1:n.789C>G
|
|
|
|
XR_928360.1:n.789C>G
|
|
|
|
XR_928361.1:n.789C>G
|
|
|
|
XR_928362.1:n.789C>G
|
|
|
|
XM_006716686.4:c.428C>G
|
XP_006716749.1:p.Thr143Arg
|
|
|
XM_011517363.3:c.407-5614C>G
|
XP_011515665.1:n.407-5614C>G
|
|
|
XM_024447326.1:c.77C>G
|
XP_024303094.1:p.Thr26Arg
|
|
|
XR_001745619.2:n.772C>G
|
|
|
|
XR_428387.2:n.772C>G
|
|
|
|
XR_928360.3:n.772C>G
|
|
|
|
XR_928362.3:n.772C>G
|
|
|
|
NM_153704.6:c.731C>G
MANE Select
|
NP_714915.3:p.Thr244Arg
|
|
|
NR_024522.2:n.752C>G
|
|
|
