ENST00000682568.1:n.1701T>A
|
|
|
ENST00000682617.1:c.1761T>A
|
ENSP00000507912.1:p.Asp587Glu
|
|
ENST00000682826.1:c.*937T>A
|
ENSP00000507274.1:n.*937T>A
|
|
ENST00000682909.1:n.3663T>A
|
|
|
ENST00000683277.1:n.3268T>A
|
|
|
ENST00000683407.1:n.1631T>A
|
|
|
ENST00000683962.1:c.*1317T>A
|
ENSP00000506854.1:n.*1317T>A
|
|
ENST00000311895.8:c.1623T>A
MANE Select
|
ENSP00000310520.7:p.Asp541Glu
|
|
ENST00000311895.7:c.1623T>A
|
ENSP00000310520.7:p.Asp541Glu
|
|
ENST00000389138.7:n.900T>A
|
|
|
NM_005236.2:c.1623T>A , LRG_463t1:c.1623T>A
|
NP_005227.1:p.Asp541Glu
|
|
XM_011522424.1:c.1761T>A
|
XP_011520726.1:p.Asp587Glu
|
|
XM_011522425.1:c.1080T>A
|
XP_011520727.1:p.Asp360Glu
|
|
XM_011522426.1:c.834T>A
|
XP_011520728.1:p.Asp278Glu
|
|
XM_011522427.1:c.273T>A
|
XP_011520729.1:p.Asp91Glu
|
|
XR_932805.1:n.1782T>A
|
|
|
XM_011522424.3:c.1761T>A
|
XP_011520726.1:p.Asp587Glu
|
|
XM_017023043.2:c.834T>A
|
XP_016878532.1:p.Asp278Glu
|
|
NM_005236.3:c.1623T>A
MANE Select
|
NP_005227.1:p.Asp541Glu
|
|