ENST00000295897.9:c.1069G>T
MANE Select
|
ENSP00000295897.4:p.Glu357Ter
|
|
ENST00000295897.8:c.1069G>T
|
ENSP00000295897.4:p.Glu357Ter
|
|
ENST00000401494.7:c.724G>T
|
ENSP00000384695.3:p.Glu242Ter
|
|
ENST00000415165.6:c.493G>T
|
ENSP00000401820.2:p.Glu165Ter
|
|
ENST00000476441.6:c.*348G>T
|
ENSP00000423727.1:n.*348G>T
|
|
ENST00000484992.1:n.389G>T
|
|
|
ENST00000503124.5:c.619G>T
|
ENSP00000421027.1:p.Glu207Ter
|
|
ENST00000504043.1:n.72G>T
|
|
|
ENST00000505649.5:n.755G>T
|
|
|
ENST00000509063.5:c.1069G>T
|
ENSP00000422784.1:p.Glu357Ter
|
|
ENST00000511370.1:c.602G>T
|
|
|
ENST00000621085.4:c.491-61G>T
|
ENSP00000483421.1:n.491-61G>T
|
|
ENST00000621628.4:c.487-57G>T
|
ENSP00000480485.1:n.487-57G>T
|
|
NM_000477.5:c.1069G>T
|
NP_000468.1:p.Glu357Ter
|
|
NM_000477.6:c.1069G>T
|
NP_000468.1:p.Glu357Ter
|
|
NM_000477.7:c.1069G>T
MANE Select
|
NP_000468.1:p.Glu357Ter
|
|