ENST00000682568.1:n.1734T>A
|
|
|
ENST00000682617.1:c.1794T>A
|
ENSP00000507912.1:p.Thr598=
|
|
ENST00000682826.1:c.*970T>A
|
ENSP00000507274.1:n.*970T>A
|
|
ENST00000682909.1:n.3696T>A
|
|
|
ENST00000683277.1:n.3301T>A
|
|
|
ENST00000683407.1:n.1664T>A
|
|
|
ENST00000683962.1:c.*1350T>A
|
ENSP00000506854.1:n.*1350T>A
|
|
ENST00000311895.8:c.1656T>A
MANE Select
|
ENSP00000310520.7:p.Thr552=
|
|
ENST00000311895.7:c.1656T>A
|
ENSP00000310520.7:p.Thr552=
|
|
ENST00000389138.7:n.933T>A
|
|
|
NM_005236.2:c.1656T>A , LRG_463t1:c.1656T>A
|
NP_005227.1:p.Thr552=
|
|
XM_011522424.1:c.1794T>A
|
XP_011520726.1:p.Thr598=
|
|
XM_011522425.1:c.1113T>A
|
XP_011520727.1:p.Thr371=
|
|
XM_011522426.1:c.867T>A
|
XP_011520728.1:p.Thr289=
|
|
XM_011522427.1:c.306T>A
|
XP_011520729.1:p.Thr102=
|
|
XR_932805.1:n.1815T>A
|
|
|
XM_011522424.3:c.1794T>A
|
XP_011520726.1:p.Thr598=
|
|
XM_017023043.2:c.867T>A
|
XP_016878532.1:p.Thr289=
|
|
NM_005236.3:c.1656T>A
MANE Select
|
NP_005227.1:p.Thr552=
|
|