|
ENST00000375766.8:c.451G>C
MANE Select
|
ENSP00000364921.3:p.Gly151Arg
|
|
|
ENST00000332305.5:c.251-1869G>C
|
ENSP00000364920.2:n.251-1869G>C
|
|
|
ENST00000375766.7:c.451G>C
|
ENSP00000364921.3:p.Gly151Arg
|
|
|
ENST00000375771.5:c.451G>C
|
ENSP00000364926.1:p.Gly151Arg
|
|
|
ENST00000441801.6:c.451G>C
|
ENSP00000416387.2:p.Gly151Arg
|
|
|
ENST00000502739.5:c.251-1869G>C
|
ENSP00000424920.1:n.251-1869G>C
|
|
|
NM_001024215.1:c.451G>C
|
NP_001019386.1:p.Gly151Arg
|
|
|
NM_001024216.1:c.251-1869G>C
|
NP_001019387.1:n.251-1869G>C
|
|
|
NM_017556.2:c.451G>C
|
NP_060026.2:p.Gly151Arg
|
|
|
XM_005245900.1:c.451G>C
|
XP_005245957.1:p.Gly151Arg
|
|
|
XM_005245901.1:c.451G>C
|
XP_005245958.1:p.Gly151Arg
|
|
|
XM_005245902.1:c.451G>C
|
XP_005245959.1:p.Gly151Arg
|
|
|
XM_005245903.1:c.451G>C
|
XP_005245960.1:p.Gly151Arg
|
|
|
XM_005245909.2:c.451G>C
|
XP_005245966.1:p.Gly151Arg
|
|
|
XM_006710704.2:c.451G>C
|
XP_006710767.1:p.Gly151Arg
|
|
|
XM_006710705.1:c.451G>C
|
XP_006710768.1:p.Gly151Arg
|
|
|
XM_011541616.1:c.451G>C
|
XP_011539918.1:p.Gly151Arg
|
|
|
XM_011541617.1:c.451G>C
|
XP_011539919.1:p.Gly151Arg
|
|
|
XM_011541618.1:c.451G>C
|
XP_011539920.1:p.Gly151Arg
|
|
|
XM_011541619.1:c.251-1869G>C
|
XP_011539921.1:n.251-1869G>C
|
|
|
XR_946670.1:n.961G>C
|
|
|
|
NM_001024216.2:c.251-1869G>C
|
NP_001019387.1:n.251-1869G>C
|
|
|
NM_001350151.1:c.451G>C
|
NP_001337080.1:p.Gly151Arg
|
|
|
NM_017556.3:c.451G>C
|
NP_060026.2:p.Gly151Arg
|
|
|
XM_006710704.3:c.451G>C
|
XP_006710767.1:p.Gly151Arg
|
|
|
XM_011541616.2:c.451G>C
|
XP_011539918.1:p.Gly151Arg
|
|
|
XM_011541617.2:c.451G>C
|
XP_011539919.1:p.Gly151Arg
|
|
|
XM_011541618.3:c.451G>C
|
XP_011539920.1:p.Gly151Arg
|
|
|
XM_017001519.2:c.451G>C
|
XP_016857008.1:p.Gly151Arg
|
|
|
XM_017001520.2:c.451G>C
|
XP_016857009.1:p.Gly151Arg
|
|
|
XM_017001521.2:c.451G>C
|
XP_016857010.1:p.Gly151Arg
|
|
|
XM_017001523.1:c.451G>C
|
XP_016857012.1:p.Gly151Arg
|
|
|
XM_017001524.1:c.451G>C
|
XP_016857013.1:p.Gly151Arg
|
|
|
XM_017001525.1:c.451G>C
|
XP_016857014.1:p.Gly151Arg
|
|
|
XM_017001526.2:c.451G>C
|
XP_016857015.1:p.Gly151Arg
|
|
|
XM_024447751.1:c.451G>C
|
XP_024303519.1:p.Gly151Arg
|
|
|
NM_017556.4:c.451G>C
MANE Select
|
NP_060026.2:p.Gly151Arg
|
|
|
NM_001024216.3:c.251-1869G>C
|
NP_001019387.1:n.251-1869G>C
|
|
|
NM_001350151.2:c.451G>C
|
NP_001337080.1:p.Gly151Arg
|
|
