ENST00000269980.7:c.735C>T
MANE Select
|
ENSP00000269980.2:p.Asp245=
|
|
ENST00000269980.6:c.735C>T
|
ENSP00000269980.2:p.Asp245=
|
|
ENST00000457836.6:c.669C>T
|
ENSP00000416000.2:p.Asp223=
|
|
ENST00000535632.5:n.364C>T
|
|
|
ENST00000540732.3:c.837C>T
|
ENSP00000443246.1:p.Asp279=
|
|
ENST00000542943.5:c.648C>T
|
ENSP00000440345.1:p.Asp216=
|
|
ENST00000545787.1:n.363C>T
|
|
|
ENST00000595085.5:c.735C>T
|
ENSP00000471150.2:p.Asp245=
|
|
NM_000709.3:c.735C>T
|
NP_000700.1:p.Asp245=
|
|
NM_001164783.1:c.735C>T
|
NP_001158255.1:p.Asp245=
|
|
NM_000709.4:c.735C>T
MANE Select
|
NP_000700.1:p.Asp245=
|
|
NM_001164783.2:c.735C>T
|
NP_001158255.1:p.Asp245=
|
|