|
ENST00000704289.1:c.*913A>T
|
ENSP00000515816.1:n.*913A>T
|
|
|
ENST00000315285.9:c.1253A>T
MANE Select
|
ENSP00000320885.3:p.Glu418Val
|
|
|
ENST00000621856.2:c.1250A>T
|
ENSP00000482496.2:p.Glu417Val
|
|
|
ENST00000642281.1:c.990A>T
|
|
|
|
ENST00000642455.1:c.1154A>T
|
ENSP00000493827.1:p.Glu385Val
|
|
|
ENST00000642751.1:c.1027A>T
|
|
|
|
ENST00000642999.1:c.995A>T
|
ENSP00000496589.1:p.Glu332Val
|
|
|
ENST00000643327.1:c.412A>T
|
|
|
|
ENST00000643334.1:c.833A>T
|
|
|
|
ENST00000644408.1:c.1129A>T
|
|
|
|
ENST00000644954.1:c.899A>T
|
ENSP00000494312.1:p.Glu300Val
|
|
|
ENST00000645159.1:n.1990A>T
|
|
|
|
ENST00000645671.1:c.703A>T
|
|
|
|
ENST00000645730.1:c.593-539A>T
|
|
|
|
ENST00000646082.1:c.899A>T
|
|
|
|
ENST00000646571.1:c.1157A>T
|
ENSP00000495015.1:p.Glu386Val
|
|
|
ENST00000647007.1:n.945A>T
|
|
|
|
ENST00000647133.1:c.753A>T
|
|
|
|
ENST00000315285.7:c.1253A>T
|
ENSP00000320885.3:p.Glu418Val
|
|
|
ENST00000345662.5:c.1157A>T
|
ENSP00000340817.1:p.Glu386Val
|
|
|
ENST00000615843.4:c.1253A>T
|
ENSP00000480893.1:p.Glu418Val
|
|
|
ENST00000621856.1:c.995A>T
|
ENSP00000482496.1:p.Glu332Val
|
|
|
NM_014946.3:c.1253A>T , LRG_714t1:c.1253A>T
|
NP_055761.2:p.Glu418Val
|
|
|
NM_199436.1:c.1157A>T
|
NP_955468.1:p.Glu386Val
|
|
|
XM_005264516.3:c.1250A>T
|
XP_005264573.1:p.Glu417Val
|
|
|
XM_011533067.1:c.1253A>T
|
XP_011531369.1:p.Glu418Val
|
|
|
NM_001363823.1:c.1250A>T
|
NP_001350752.1:p.Glu417Val
|
|
|
NM_001363875.1:c.1154A>T
|
NP_001350804.1:p.Glu385Val
|
|
|
XM_005264516.5:c.1250A>T
|
XP_005264573.1:p.Glu417Val
|
|
|
XM_011533067.2:c.1253A>T
|
XP_011531369.1:p.Glu418Val
|
|
|
XM_017004778.2:c.1157A>T
|
XP_016860267.1:p.Glu386Val
|
|
|
NM_001363823.2:c.1250A>T
|
NP_001350752.1:p.Glu417Val
|
|
|
NM_001363875.2:c.1154A>T
|
NP_001350804.1:p.Glu385Val
|
|
|
NM_001377959.1:c.1157A>T
|
NP_001364888.1:p.Glu386Val
|
|
|
NM_014946.4:c.1253A>T
MANE Select
|
NP_055761.2:p.Glu418Val
|
|
|
NM_199436.2:c.1157A>T
|
NP_955468.1:p.Glu386Val
|
|
