ENST00000465218.3:n.617A>T
|
|
|
ENST00000468748.7:n.577A>T
|
|
|
ENST00000484154.2:n.1215A>T
|
|
|
ENST00000491008.6:n.1342A>T
|
|
|
ENST00000492226.2:n.591A>T
|
|
|
ENST00000492773.6:c.326A>T
|
|
|
ENST00000647636.1:c.594A>T
|
ENSP00000497505.1:p.Glu198Asp
|
|
ENST00000647909.1:c.618A>T
|
ENSP00000498164.1:p.Glu206Asp
|
|
ENST00000648145.1:c.362A>T
|
|
|
ENST00000648189.1:c.344A>T
|
|
|
ENST00000648256.1:c.543A>T
|
ENSP00000497356.1:p.Glu181Asp
|
|
ENST00000648314.1:c.594A>T
|
ENSP00000496920.1:p.Glu198Asp
|
|
ENST00000648599.1:c.594A>T
|
ENSP00000497159.1:p.Glu198Asp
|
|
ENST00000648630.1:c.588A>T
|
ENSP00000497887.1:p.Glu196Asp
|
|
ENST00000648682.1:c.594A>T
|
ENSP00000498185.1:p.Glu198Asp
|
|
ENST00000648882.1:c.*420A>T
|
ENSP00000497603.1:n.*420A>T
|
|
ENST00000648890.1:c.594A>T
|
ENSP00000497503.1:p.Glu198Asp
|
|
ENST00000648915.2:c.594A>T
MANE Select
|
ENSP00000497160.1:p.Glu198Asp
|
|
ENST00000649545.1:c.328A>T
|
|
|
ENST00000649688.1:c.594A>T
|
ENSP00000497097.1:p.Glu198Asp
|
|
ENST00000649814.1:n.643A>T
|
|
|
ENST00000650270.1:c.461A>T
|
|
|
ENST00000273783.7:c.594A>T
|
ENSP00000273783.3:p.Glu198Asp
|
|
ENST00000432982.5:c.245+1310A>T
|
|
|
ENST00000444495.1:c.594A>T
|
ENSP00000409142.1:p.Glu198Asp
|
|
ENST00000468748.5:n.47A>T
|
|
|
ENST00000481054.5:n.595A>T
|
|
|
ENST00000491008.5:n.558A>T
|
|
|
ENST00000491144.5:n.1034A>T
|
|
|
ENST00000498831.1:n.549A>T
|
|
|
NM_003907.2:c.594A>T
|
NP_003898.2:p.Glu198Asp
|
|
XR_924208.1:n.1545A>T
|
|
|
NM_003907.3:c.594A>T
MANE Select
|
NP_003898.2:p.Glu198Asp
|
|
XM_011513266.3:c.-308A>T
|
XP_011511568.1:n.-308A>T
|
|
XR_001740352.2:n.957A>T
|
|
|
XR_001740353.2:n.957A>T
|
|
|
XR_924208.2:n.957A>T
|
|
|