|
ENST00000704289.1:c.*827A>T
|
ENSP00000515816.1:n.*827A>T
|
|
|
ENST00000315285.9:c.1167A>T
MANE Select
|
ENSP00000320885.3:p.Thr389=
|
|
|
ENST00000621856.2:c.1164A>T
|
ENSP00000482496.2:p.Thr388=
|
|
|
ENST00000642281.1:c.983-9547A>T
|
|
|
|
ENST00000642455.1:c.1068A>T
|
ENSP00000493827.1:p.Thr356=
|
|
|
ENST00000642751.1:c.941A>T
|
|
|
|
ENST00000642999.1:c.909A>T
|
ENSP00000496589.1:p.Thr303=
|
|
|
ENST00000643327.1:c.326A>T
|
|
|
|
ENST00000643334.1:c.747A>T
|
|
|
|
ENST00000644408.1:c.1043A>T
|
|
|
|
ENST00000644954.1:c.813A>T
|
ENSP00000494312.1:p.Thr271=
|
|
|
ENST00000645159.1:n.519A>T
|
|
|
|
ENST00000645550.1:n.380A>T
|
|
|
|
ENST00000645671.1:c.617A>T
|
|
|
|
ENST00000645730.1:c.514A>T
|
|
|
|
ENST00000646082.1:c.813A>T
|
|
|
|
ENST00000646571.1:c.1071A>T
|
ENSP00000495015.1:p.Thr357=
|
|
|
ENST00000647007.1:n.859A>T
|
|
|
|
ENST00000647133.1:c.674-1392A>T
|
|
|
|
ENST00000315285.7:c.1167A>T
|
ENSP00000320885.3:p.Thr389=
|
|
|
ENST00000345662.5:c.1071A>T
|
ENSP00000340817.1:p.Thr357=
|
|
|
ENST00000615843.4:c.1167A>T
|
ENSP00000480893.1:p.Thr389=
|
|
|
ENST00000621856.1:c.909A>T
|
ENSP00000482496.1:p.Thr303=
|
|
|
NM_014946.3:c.1167A>T , LRG_714t1:c.1167A>T
|
NP_055761.2:p.Thr389=
|
|
|
NM_199436.1:c.1071A>T
|
NP_955468.1:p.Thr357=
|
|
|
XM_005264516.3:c.1164A>T
|
XP_005264573.1:p.Thr388=
|
|
|
XM_011533067.1:c.1167A>T
|
XP_011531369.1:p.Thr389=
|
|
|
NM_001363823.1:c.1164A>T
|
NP_001350752.1:p.Thr388=
|
|
|
NM_001363875.1:c.1068A>T
|
NP_001350804.1:p.Thr356=
|
|
|
XM_005264516.5:c.1164A>T
|
XP_005264573.1:p.Thr388=
|
|
|
XM_011533067.2:c.1167A>T
|
XP_011531369.1:p.Thr389=
|
|
|
XM_017004778.2:c.1071A>T
|
XP_016860267.1:p.Thr357=
|
|
|
NM_001363823.2:c.1164A>T
|
NP_001350752.1:p.Thr388=
|
|
|
NM_001363875.2:c.1068A>T
|
NP_001350804.1:p.Thr356=
|
|
|
NM_001377959.1:c.1071A>T
|
NP_001364888.1:p.Thr357=
|
|
|
NM_014946.4:c.1167A>T
MANE Select
|
NP_055761.2:p.Thr389=
|
|
|
NM_199436.2:c.1071A>T
|
NP_955468.1:p.Thr357=
|
|
