ENST00000295897.9:c.1780G>T
MANE Select
|
ENSP00000295897.4:p.Glu594Ter
|
|
ENST00000295897.8:c.1780G>T
|
ENSP00000295897.4:p.Glu594Ter
|
|
ENST00000401494.7:c.1435G>T
|
ENSP00000384695.3:p.Glu479Ter
|
|
ENST00000415165.6:c.1204G>T
|
ENSP00000401820.2:p.Glu402Ter
|
|
ENST00000476441.6:c.*1059G>T
|
ENSP00000423727.1:n.*1059G>T
|
|
ENST00000495173.1:n.88G>T
|
|
|
ENST00000503124.5:c.1330G>T
|
ENSP00000421027.1:p.Glu444Ter
|
|
ENST00000505649.5:n.1327G>T
|
|
|
ENST00000508932.5:n.175+179G>T
|
|
|
ENST00000509063.5:c.1780G>T
|
ENSP00000422784.1:p.Glu594Ter
|
|
ENST00000511370.1:c.1313G>T
|
|
|
ENST00000621085.4:c.1141G>T
|
ENSP00000483421.1:p.Glu381Ter
|
|
ENST00000621628.4:c.1141G>T
|
ENSP00000480485.1:p.Glu381Ter
|
|
NM_000477.5:c.1780G>T
|
NP_000468.1:p.Glu594Ter
|
|
NM_000477.6:c.1780G>T
|
NP_000468.1:p.Glu594Ter
|
|
NM_000477.7:c.1780G>T
MANE Select
|
NP_000468.1:p.Glu594Ter
|
|