|
ENST00000704289.1:c.*825A>G
|
ENSP00000515816.1:n.*825A>G
|
|
|
ENST00000315285.9:c.1165A>G
MANE Select
|
ENSP00000320885.3:p.Thr389Ala
|
|
|
ENST00000621856.2:c.1162A>G
|
ENSP00000482496.2:p.Thr388Ala
|
|
|
ENST00000642281.1:c.983-9549A>G
|
|
|
|
ENST00000642455.1:c.1066A>G
|
ENSP00000493827.1:p.Thr356Ala
|
|
|
ENST00000642751.1:c.939A>G
|
|
|
|
ENST00000642999.1:c.907A>G
|
ENSP00000496589.1:p.Thr303Ala
|
|
|
ENST00000643327.1:c.324A>G
|
|
|
|
ENST00000643334.1:c.745A>G
|
|
|
|
ENST00000644408.1:c.1041A>G
|
|
|
|
ENST00000644954.1:c.811A>G
|
ENSP00000494312.1:p.Thr271Ala
|
|
|
ENST00000645159.1:n.517A>G
|
|
|
|
ENST00000645550.1:n.378A>G
|
|
|
|
ENST00000645671.1:c.615A>G
|
|
|
|
ENST00000645730.1:c.512A>G
|
|
|
|
ENST00000646082.1:c.811A>G
|
|
|
|
ENST00000646571.1:c.1069A>G
|
ENSP00000495015.1:p.Thr357Ala
|
|
|
ENST00000647007.1:n.857A>G
|
|
|
|
ENST00000647133.1:c.674-1394A>G
|
|
|
|
ENST00000315285.7:c.1165A>G
|
ENSP00000320885.3:p.Thr389Ala
|
|
|
ENST00000345662.5:c.1069A>G
|
ENSP00000340817.1:p.Thr357Ala
|
|
|
ENST00000615843.4:c.1165A>G
|
ENSP00000480893.1:p.Thr389Ala
|
|
|
ENST00000621856.1:c.907A>G
|
ENSP00000482496.1:p.Thr303Ala
|
|
|
NM_014946.3:c.1165A>G , LRG_714t1:c.1165A>G
|
NP_055761.2:p.Thr389Ala
|
|
|
NM_199436.1:c.1069A>G
|
NP_955468.1:p.Thr357Ala
|
|
|
XM_005264516.3:c.1162A>G
|
XP_005264573.1:p.Thr388Ala
|
|
|
XM_011533067.1:c.1165A>G
|
XP_011531369.1:p.Thr389Ala
|
|
|
NM_001363823.1:c.1162A>G
|
NP_001350752.1:p.Thr388Ala
|
|
|
NM_001363875.1:c.1066A>G
|
NP_001350804.1:p.Thr356Ala
|
|
|
XM_005264516.5:c.1162A>G
|
XP_005264573.1:p.Thr388Ala
|
|
|
XM_011533067.2:c.1165A>G
|
XP_011531369.1:p.Thr389Ala
|
|
|
XM_017004778.2:c.1069A>G
|
XP_016860267.1:p.Thr357Ala
|
|
|
NM_001363823.2:c.1162A>G
|
NP_001350752.1:p.Thr388Ala
|
|
|
NM_001363875.2:c.1066A>G
|
NP_001350804.1:p.Thr356Ala
|
|
|
NM_001377959.1:c.1069A>G
|
NP_001364888.1:p.Thr357Ala
|
|
|
NM_014946.4:c.1165A>G
MANE Select
|
NP_055761.2:p.Thr389Ala
|
|
|
NM_199436.2:c.1069A>G
|
NP_955468.1:p.Thr357Ala
|
|
