|
ENST00000704289.1:c.*806T>C
|
ENSP00000515816.1:n.*806T>C
|
|
|
ENST00000315285.9:c.1146T>C
MANE Select
|
ENSP00000320885.3:p.Gly382=
|
|
|
ENST00000621856.2:c.1143T>C
|
ENSP00000482496.2:p.Gly381=
|
|
|
ENST00000642281.1:c.983-9568T>C
|
|
|
|
ENST00000642455.1:c.1047T>C
|
ENSP00000493827.1:p.Gly349=
|
|
|
ENST00000642751.1:c.920T>C
|
|
|
|
ENST00000642999.1:c.888T>C
|
ENSP00000496589.1:p.Gly296=
|
|
|
ENST00000643327.1:c.305T>C
|
|
|
|
ENST00000643334.1:c.726T>C
|
|
|
|
ENST00000644408.1:c.1022T>C
|
|
|
|
ENST00000644954.1:c.792T>C
|
ENSP00000494312.1:p.Gly264=
|
|
|
ENST00000645159.1:n.498T>C
|
|
|
|
ENST00000645550.1:n.359T>C
|
|
|
|
ENST00000645671.1:c.596T>C
|
|
|
|
ENST00000645730.1:c.493T>C
|
|
|
|
ENST00000646082.1:c.792T>C
|
|
|
|
ENST00000646571.1:c.1050T>C
|
ENSP00000495015.1:p.Gly350=
|
|
|
ENST00000647007.1:n.838T>C
|
|
|
|
ENST00000647133.1:c.674-1413T>C
|
|
|
|
ENST00000315285.7:c.1146T>C
|
ENSP00000320885.3:p.Gly382=
|
|
|
ENST00000345662.5:c.1050T>C
|
ENSP00000340817.1:p.Gly350=
|
|
|
ENST00000615843.4:c.1146T>C
|
ENSP00000480893.1:p.Gly382=
|
|
|
ENST00000621856.1:c.888T>C
|
ENSP00000482496.1:p.Gly296=
|
|
|
NM_014946.3:c.1146T>C , LRG_714t1:c.1146T>C
|
NP_055761.2:p.Gly382=
|
|
|
NM_199436.1:c.1050T>C
|
NP_955468.1:p.Gly350=
|
|
|
XM_005264516.3:c.1143T>C
|
XP_005264573.1:p.Gly381=
|
|
|
XM_011533067.1:c.1146T>C
|
XP_011531369.1:p.Gly382=
|
|
|
NM_001363823.1:c.1143T>C
|
NP_001350752.1:p.Gly381=
|
|
|
NM_001363875.1:c.1047T>C
|
NP_001350804.1:p.Gly349=
|
|
|
XM_005264516.5:c.1143T>C
|
XP_005264573.1:p.Gly381=
|
|
|
XM_011533067.2:c.1146T>C
|
XP_011531369.1:p.Gly382=
|
|
|
XM_017004778.2:c.1050T>C
|
XP_016860267.1:p.Gly350=
|
|
|
NM_001363823.2:c.1143T>C
|
NP_001350752.1:p.Gly381=
|
|
|
NM_001363875.2:c.1047T>C
|
NP_001350804.1:p.Gly349=
|
|
|
NM_001377959.1:c.1050T>C
|
NP_001364888.1:p.Gly350=
|
|
|
NM_014946.4:c.1146T>C
MANE Select
|
NP_055761.2:p.Gly382=
|
|
|
NM_199436.2:c.1050T>C
|
NP_955468.1:p.Gly350=
|
|
