|
ENST00000382099.3:c.1679A>T
|
|
|
|
ENST00000382100.8:c.2121A>T
MANE Select
|
ENSP00000371532.2:p.Glu707Asp
|
|
|
ENST00000679488.1:n.1547A>T
|
|
|
|
ENST00000679718.1:n.1357A>T
|
|
|
|
ENST00000679750.1:n.1537A>T
|
|
|
|
ENST00000679780.1:n.897A>T
|
|
|
|
ENST00000679851.1:n.2920A>T
|
|
|
|
ENST00000680021.1:n.2321A>T
|
|
|
|
ENST00000680043.1:c.1673A>T
|
|
|
|
ENST00000680219.1:c.1688A>T
|
|
|
|
ENST00000680243.1:c.*1760A>T
|
ENSP00000505911.1:n.*1760A>T
|
|
|
ENST00000680296.1:c.1547A>T
|
|
|
|
ENST00000680332.1:n.1754A>T
|
|
|
|
ENST00000680440.1:n.261A>T
|
|
|
|
ENST00000680746.1:c.1998A>T
|
ENSP00000505030.1:p.Glu666Asp
|
|
|
ENST00000680751.1:n.1526A>T
|
|
|
|
ENST00000680891.1:c.*1913A>T
|
ENSP00000505167.1:n.*1913A>T
|
|
|
ENST00000680975.1:n.1506A>T
|
|
|
|
ENST00000681087.1:n.1426A>T
|
|
|
|
ENST00000681306.1:c.2121A>T
|
ENSP00000506072.1:p.Glu707Asp
|
|
|
ENST00000681486.1:n.221A>T
|
|
|
|
ENST00000681618.1:c.1998A>T
|
ENSP00000505773.1:p.Glu666Asp
|
|
|
ENST00000681644.1:c.*1793A>T
|
ENSP00000505180.1:n.*1793A>T
|
|
|
ENST00000681806.1:c.*559A>T
|
ENSP00000505282.1:n.*559A>T
|
|
|
ENST00000681942.1:c.1604A>T
|
|
|
|
ENST00000382099.2:c.2121A>T
|
ENSP00000371531.2:p.Glu707Asp
|
|
|
ENST00000382100.7:c.2121A>T
|
ENSP00000371532.2:p.Glu707Asp
|
|
|
NM_001018056.1:c.2121A>T
|
NP_001018066.1:p.Glu707Asp
|
|
|
NM_003383.3:c.2121A>T
|
NP_003374.3:p.Glu707Asp
|
|
|
XM_011518029.1:c.1998A>T
|
XP_011516331.1:p.Glu666Asp
|
|
|
NM_001018056.2:c.2121A>T
|
NP_001018066.1:p.Glu707Asp
|
|
|
NM_001322225.1:c.1998A>T
|
NP_001309154.1:p.Glu666Asp
|
|
|
NM_001322226.1:c.1998A>T
|
NP_001309155.1:p.Glu666Asp
|
|
|
NM_003383.4:c.2121A>T
|
NP_003374.3:p.Glu707Asp
|
|
|
XR_001746373.2:n.2460A>T
|
|
|
|
XR_002956805.1:n.2460A>T
|
|
|
|
NM_003383.5:c.2121A>T
MANE Select
|
NP_003374.3:p.Glu707Asp
|
|
|
NM_001018056.3:c.2121A>T
|
NP_001018066.1:p.Glu707Asp
|
|
|
NM_001322225.2:c.1998A>T
|
NP_001309154.1:p.Glu666Asp
|
|
|
NM_001322226.2:c.1998A>T
|
NP_001309155.1:p.Glu666Asp
|
|
