ENST00000382099.3:c.937A>T
|
|
|
ENST00000382100.8:c.1379A>T
MANE Select
|
ENSP00000371532.2:p.Glu460Val
|
|
ENST00000478776.2:n.824A>T
|
|
|
ENST00000679718.1:n.615A>T
|
|
|
ENST00000679750.1:n.795A>T
|
|
|
ENST00000679851.1:n.1563A>T
|
|
|
ENST00000680021.1:n.1579A>T
|
|
|
ENST00000680043.1:c.931A>T
|
|
|
ENST00000680219.1:c.946A>T
|
|
|
ENST00000680243.1:c.*1158A>T
|
ENSP00000505911.1:n.*1158A>T
|
|
ENST00000680296.1:c.805A>T
|
|
|
ENST00000680332.1:n.462A>T
|
|
|
ENST00000680746.1:c.1256A>T
|
ENSP00000505030.1:p.Glu419Val
|
|
ENST00000680751.1:n.784A>T
|
|
|
ENST00000680891.1:c.*1171A>T
|
ENSP00000505167.1:n.*1171A>T
|
|
ENST00000680975.1:n.764A>T
|
|
|
ENST00000681087.1:n.824A>T
|
|
|
ENST00000681306.1:c.1379A>T
|
ENSP00000506072.1:p.Glu460Val
|
|
ENST00000681618.1:c.1256A>T
|
ENSP00000505773.1:p.Glu419Val
|
|
ENST00000681644.1:c.*1051A>T
|
ENSP00000505180.1:n.*1051A>T
|
|
ENST00000681806.1:c.1379A>T
|
ENSP00000505282.1:p.Glu460Val
|
|
ENST00000681942.1:c.927A>T
|
|
|
ENST00000382099.2:c.1379A>T
|
ENSP00000371531.2:p.Glu460Val
|
|
ENST00000382100.7:c.1379A>T
|
ENSP00000371532.2:p.Glu460Val
|
|
NM_001018056.1:c.1379A>T
|
NP_001018066.1:p.Glu460Val
|
|
NM_003383.3:c.1379A>T
|
NP_003374.3:p.Glu460Val
|
|
XM_011518029.1:c.1256A>T
|
XP_011516331.1:p.Glu419Val
|
|
NM_001018056.2:c.1379A>T
|
NP_001018066.1:p.Glu460Val
|
|
NM_001322225.1:c.1256A>T
|
NP_001309154.1:p.Glu419Val
|
|
NM_001322226.1:c.1256A>T
|
NP_001309155.1:p.Glu419Val
|
|
NM_003383.4:c.1379A>T
|
NP_003374.3:p.Glu460Val
|
|
XR_001746373.2:n.1783A>T
|
|
|
XR_002956805.1:n.1783A>T
|
|
|
NM_003383.5:c.1379A>T
MANE Select
|
NP_003374.3:p.Glu460Val
|
|
NM_001018056.3:c.1379A>T
|
NP_001018066.1:p.Glu460Val
|
|
NM_001322225.2:c.1256A>T
|
NP_001309154.1:p.Glu419Val
|
|
NM_001322226.2:c.1256A>T
|
NP_001309155.1:p.Glu419Val
|
|