|
ENST00000323130.8:c.763A>G
|
ENSP00000314488.4:p.Met255Val
|
|
|
ENST00000409623.8:c.763A>G
|
ENSP00000386966.4:p.Met255Val
|
|
|
ENST00000452276.6:c.763A>G
|
ENSP00000388671.2:p.Met255Val
|
|
|
ENST00000453906.6:c.407-5582A>G
|
ENSP00000403035.2:n.407-5582A>G
|
|
|
ENST00000520680.2:c.763A>G
|
ENSP00000428785.2:p.Met255Val
|
|
|
ENST00000521065.2:c.*480A>G
|
ENSP00000427947.2:n.*480A>G
|
|
|
ENST00000521517.6:c.763A>G
|
ENSP00000430740.2:p.Met255Val
|
|
|
ENST00000681998.1:c.693A>G
|
ENSP00000506773.1:n.693A>G
|
|
|
ENST00000682036.1:c.407-5582A>G
|
ENSP00000508390.1:n.407-5582A>G
|
|
|
ENST00000682577.1:c.693A>G
|
ENSP00000506963.1:n.693A>G
|
|
|
ENST00000682624.1:c.*337A>G
|
ENSP00000508343.1:n.*337A>G
|
|
|
ENST00000682700.1:c.763A>G
|
ENSP00000507627.1:p.Met255Val
|
|
|
ENST00000682744.1:n.301A>G
|
|
|
|
ENST00000682804.1:n.586A>G
|
|
|
|
ENST00000682837.1:c.518A>G
|
ENSP00000507920.1:p.Asp173Gly
|
|
|
ENST00000682935.1:n.2323A>G
|
|
|
|
ENST00000682984.1:c.424A>G
|
ENSP00000507209.1:p.Met142Val
|
|
|
ENST00000683078.1:c.518A>G
|
ENSP00000506796.1:p.Asp173Gly
|
|
|
ENST00000683223.1:c.604A>G
|
ENSP00000507685.1:n.604A>G
|
|
|
ENST00000683238.1:n.2144A>G
|
|
|
|
ENST00000683249.1:n.2344A>G
|
|
|
|
ENST00000683336.1:c.693A>G
|
ENSP00000507695.1:n.693A>G
|
|
|
ENST00000683362.1:c.424A>G
|
ENSP00000506985.1:p.Met142Val
|
|
|
ENST00000683850.1:n.686A>G
|
|
|
|
ENST00000683919.1:c.693A>G
|
ENSP00000507617.1:n.693A>G
|
|
|
ENST00000683953.1:c.674A>G
|
ENSP00000508375.1:n.674A>G
|
|
|
ENST00000684023.1:c.897A>G
|
ENSP00000507461.1:n.897A>G
|
|
|
ENST00000684064.1:c.454A>G
|
ENSP00000508192.1:p.Met152Val
|
|
|
ENST00000684089.1:n.2313A>G
|
|
|
|
ENST00000684149.1:c.*99A>G
|
ENSP00000507943.1:n.*99A>G
|
|
|
ENST00000684416.1:n.722A>G
|
|
|
|
ENST00000684540.1:c.693A>G
|
ENSP00000507987.1:n.693A>G
|
|
|
ENST00000453321.8:c.763A>G
MANE Select
|
ENSP00000389998.3:p.Met255Val
|
|
|
ENST00000323130.7:c.733A>G
|
ENSP00000314488.3:p.Met245Val
|
|
|
ENST00000409623.7:c.520A>G
|
ENSP00000386966.3:p.Met174Val
|
|
|
ENST00000425545.2:n.210A>G
|
|
|
|
ENST00000452276.5:c.454A>G
|
ENSP00000388671.1:p.Met152Val
|
|
|
ENST00000453321.7:c.763A>G
|
ENSP00000389998.3:p.Met255Val
|
|
|
ENST00000453906.5:c.407-5582A>G
|
ENSP00000403035.1:n.407-5582A>G
|
|
|
ENST00000474944.5:n.427-5582A>G
|
|
|
|
ENST00000496213.5:n.228A>G
|
|
|
|
NM_001142301.1:c.520A>G , LRG_688t2:c.520A>G
|
NP_001135773.1:p.Met174Val
|
|
|
NM_153704.5:c.763A>G , LRG_688t1:c.763A>G
|
NP_714915.3:p.Met255Val
|
|
|
NR_024522.1:n.834A>G
|
|
|
|
XM_006716686.2:c.460A>G
|
XP_006716749.1:p.Met154Val
|
|
|
XM_006716687.2:c.163A>G
|
XP_006716750.1:p.Met55Val
|
|
|
XM_011517363.1:c.407-5582A>G
|
XP_011515665.1:n.407-5582A>G
|
|
|
XR_428387.1:n.821A>G
|
|
|
|
XR_928360.1:n.821A>G
|
|
|
|
XR_928361.1:n.821A>G
|
|
|
|
XR_928362.1:n.821A>G
|
|
|
|
XM_006716686.4:c.460A>G
|
XP_006716749.1:p.Met154Val
|
|
|
XM_011517363.3:c.407-5582A>G
|
XP_011515665.1:n.407-5582A>G
|
|
|
XM_024447326.1:c.109A>G
|
XP_024303094.1:p.Met37Val
|
|
|
XR_001745619.2:n.804A>G
|
|
|
|
XR_428387.2:n.804A>G
|
|
|
|
XR_928360.3:n.804A>G
|
|
|
|
XR_928362.3:n.804A>G
|
|
|
|
NM_153704.6:c.763A>G
MANE Select
|
NP_714915.3:p.Met255Val
|
|
|
NR_024522.2:n.784A>G
|
|
|
