ENST00000465011.2:c.*1066G>T
|
ENSP00000419009.1:n.*1066G>T
|
|
ENST00000467655.2:c.*518G>T
|
ENSP00000418547.2:n.*518G>T
|
|
ENST00000704365.1:c.1431G>T
|
ENSP00000515873.1:p.Glu477Asp
|
|
ENST00000704366.1:c.1329G>T
|
ENSP00000515874.1:p.Glu443Asp
|
|
ENST00000704367.1:c.1152G>T
|
ENSP00000515875.1:p.Glu384Asp
|
|
ENST00000704368.1:n.1924G>T
|
|
|
ENST00000704369.1:c.945G>T
|
ENSP00000515876.1:p.Glu315Asp
|
|
ENST00000704370.1:c.1425G>T
|
ENSP00000515877.1:p.Glu475Asp
|
|
ENST00000704372.1:n.1785G>T
|
|
|
ENST00000704444.1:c.1215G>T
|
ENSP00000515896.1:p.Glu405Asp
|
|
ENST00000704445.1:c.1083G>T
|
ENSP00000515897.1:p.Glu361Asp
|
|
ENST00000704446.1:c.1048+841G>T
|
ENSP00000515898.1:n.1048+841G>T
|
|
ENST00000341893.8:c.1431G>T
MANE Select
|
ENSP00000342510.3:p.Glu477Asp
|
|
ENST00000341893.7:c.1431G>T
|
ENSP00000342510.3:p.Glu477Asp
|
|
ENST00000467655.1:c.1046G>T
|
ENSP00000418547.1:n.1046G>T
|
|
ENST00000489172.5:n.1413G>T
|
|
|
ENST00000494050.5:c.1254G>T
|
ENSP00000418185.1:p.Glu418Asp
|
|
NM_001303401.1:c.1254G>T
|
NP_001290330.1:p.Glu418Asp
|
|
NM_024548.3:c.1431G>T
|
NP_078824.2:p.Glu477Asp
|
|
XM_006713743.2:c.1329G>T
|
XP_006713806.1:p.Glu443Asp
|
|
XM_011513125.1:c.1215G>T
|
XP_011511427.1:p.Glu405Asp
|
|
XM_011513126.1:c.1215G>T
|
XP_011511428.1:p.Glu405Asp
|
|
XM_011513127.1:c.1083G>T
|
XP_011511429.1:p.Glu361Asp
|
|
XM_006713743.4:c.1329G>T
|
XP_006713806.1:p.Glu443Asp
|
|
XM_017007178.2:c.1152G>T
|
XP_016862667.1:p.Glu384Asp
|
|
NM_024548.4:c.1431G>T
MANE Select
|
NP_078824.2:p.Glu477Asp
|
|
NM_001303401.2:c.1254G>T
|
NP_001290330.1:p.Glu418Asp
|
|