|
ENST00000440940.7:c.594T>G
MANE Select
|
ENSP00000402510.2:p.Asp198Glu
|
|
|
ENST00000264668.6:c.675T>G
|
ENSP00000264668.2:p.Asp225Glu
|
|
|
ENST00000440940.6:c.594T>G
|
ENSP00000402510.2:p.Asp198Glu
|
|
|
ENST00000510279.5:c.*263T>G
|
ENSP00000427200.1:n.*263T>G
|
|
|
ENST00000510525.5:c.619T>G
|
|
|
|
ENST00000511461.5:c.507T>G
|
|
|
|
ENST00000513439.5:c.*301T>G
|
ENSP00000426710.1:n.*301T>G
|
|
|
ENST00000514220.5:c.379T>G
|
|
|
|
ENST00000514369.5:c.*258T>G
|
ENSP00000426132.1:n.*258T>G
|
|
|
NM_002454.2:c.594T>G
|
NP_002445.2:p.Asp198Glu
|
|
|
NM_024010.2:c.675T>G
|
NP_076915.2:p.Asp225Glu
|
|
|
XM_006714474.2:c.675T>G
|
XP_006714537.1:p.Asp225Glu
|
|
|
XM_011514043.1:c.675T>G
|
XP_011512345.1:p.Asp225Glu
|
|
|
XM_011514044.1:c.594T>G
|
XP_011512346.1:p.Asp198Glu
|
|
|
XM_011514045.1:c.675T>G
|
XP_011512347.1:p.Asp225Glu
|
|
|
XR_241702.1:n.697T>G
|
|
|
|
XR_241703.1:n.690T>G
|
|
|
|
XR_925614.1:n.697T>G
|
|
|
|
XR_925615.1:n.697T>G
|
|
|
|
NM_001364440.1:c.594T>G
|
NP_001351369.1:p.Asp198Glu
|
|
|
NM_001364441.1:c.594T>G
|
NP_001351370.1:p.Asp198Glu
|
|
|
NM_001364442.1:c.594T>G
|
NP_001351371.1:p.Asp198Glu
|
|
|
NM_024010.3:c.594T>G
|
NP_076915.3:p.Asp198Glu
|
|
|
NR_134480.1:n.717T>G
|
|
|
|
NR_134481.1:n.731T>G
|
|
|
|
NR_134482.1:n.577T>G
|
|
|
|
NR_157168.1:n.647T>G
|
|
|
|
NR_157169.1:n.507T>G
|
|
|
|
NR_157170.1:n.533T>G
|
|
|
|
NR_157171.1:n.507T>G
|
|
|
|
NR_157172.1:n.533T>G
|
|
|
|
NR_157173.1:n.661T>G
|
|
|
|
NR_157174.1:n.533T>G
|
|
|
|
NR_157175.1:n.687T>G
|
|
|
|
NR_157176.1:n.687T>G
|
|
|
|
NR_157177.1:n.682T>G
|
|
|
|
NR_157178.1:n.687T>G
|
|
|
|
XM_024446063.1:c.639T>G
|
XP_024301831.1:p.Asp213Glu
|
|
|
XM_024446064.1:c.594T>G
|
XP_024301832.1:p.Asp198Glu
|
|
|
XR_001742071.1:n.697T>G
|
|
|
|
XR_001742072.1:n.697T>G
|
|
|
|
XR_001742074.1:n.697T>G
|
|
|
|
XR_001742075.1:n.697T>G
|
|
|
|
XR_001742076.1:n.697T>G
|
|
|
|
XR_001742077.1:n.697T>G
|
|
|
|
NM_001364440.2:c.594T>G
|
NP_001351369.1:p.Asp198Glu
|
|
|
NM_001364441.2:c.594T>G
|
NP_001351370.1:p.Asp198Glu
|
|
|
NM_001364442.2:c.594T>G
|
NP_001351371.1:p.Asp198Glu
|
|
|
NM_002454.3:c.594T>G
MANE Select
|
NP_002445.2:p.Asp198Glu
|
|
|
NM_024010.4:c.594T>G
|
NP_076915.3:p.Asp198Glu
|
|
|
NR_134480.2:n.673T>G
|
|
|
|
NR_134481.2:n.687T>G
|
|
|
|
NR_134482.2:n.533T>G
|
|
|
|
NR_157168.2:n.647T>G
|
|
|
|
NR_157169.2:n.507T>G
|
|
|
|
NR_157170.2:n.533T>G
|
|
|
|
NR_157171.2:n.507T>G
|
|
|
|
NR_157172.2:n.533T>G
|
|
|
|
NR_157173.2:n.661T>G
|
|
|
|
NR_157174.2:n.533T>G
|
|
|
|
NR_157175.2:n.687T>G
|
|
|
|
NR_157176.2:n.687T>G
|
|
|
|
NR_157177.2:n.682T>G
|
|
|
|
NR_157178.2:n.687T>G
|
|
|
