ENST00000682568.1:n.1793A>T
|
|
|
ENST00000682617.1:c.1853A>T
|
ENSP00000507912.1:p.Glu618Val
|
|
ENST00000682826.1:c.*1029A>T
|
ENSP00000507274.1:n.*1029A>T
|
|
ENST00000682909.1:n.3755A>T
|
|
|
ENST00000683277.1:n.3360A>T
|
|
|
ENST00000683407.1:n.1723A>T
|
|
|
ENST00000683962.1:c.*1409A>T
|
ENSP00000506854.1:n.*1409A>T
|
|
ENST00000311895.8:c.1715A>T
MANE Select
|
ENSP00000310520.7:p.Glu572Val
|
|
ENST00000311895.7:c.1715A>T
|
ENSP00000310520.7:p.Glu572Val
|
|
ENST00000389138.7:n.992A>T
|
|
|
NM_005236.2:c.1715A>T , LRG_463t1:c.1715A>T
|
NP_005227.1:p.Glu572Val
|
|
XM_011522424.1:c.1853A>T
|
XP_011520726.1:p.Glu618Val
|
|
XM_011522425.1:c.1172A>T
|
XP_011520727.1:p.Glu391Val
|
|
XM_011522426.1:c.926A>T
|
XP_011520728.1:p.Glu309Val
|
|
XM_011522427.1:c.365A>T
|
XP_011520729.1:p.Glu122Val
|
|
XR_932805.1:n.1874A>T
|
|
|
XM_011522424.3:c.1853A>T
|
XP_011520726.1:p.Glu618Val
|
|
XM_017023043.2:c.926A>T
|
XP_016878532.1:p.Glu309Val
|
|
NM_005236.3:c.1715A>T
MANE Select
|
NP_005227.1:p.Glu572Val
|
|