ENST00000333628.4:c.421_422del
MANE Select
|
ENSP00000369703.2:p.Gly141ArgfsTer?
|
|
ENST00000679400.1:n.477_478del
|
|
|
ENST00000679907.1:n.809_810del
|
|
|
ENST00000680036.1:n.1203_1204del
|
|
|
ENST00000680967.1:n.1511_1512del
|
|
|
ENST00000333628.3:c.421_422del
|
ENSP00000369703.2:p.Gly141ArgfsTer?
|
|
ENST00000489942.1:n.616_617del
|
|
|
NM_001069.2:c.421_422del
|
NP_001060.1:p.Gly141ArgfsTer?
|
|
NM_001310315.1:c.166_167del
|
NP_001297244.1:p.Gly56ArgfsTer?
|
|
NM_001069.3:c.421_422del
MANE Select
|
NP_001060.1:p.Gly141ArgfsTer?
|
|
NM_001310315.2:c.166_167del
|
NP_001297244.1:p.Gly56ArgfsTer?
|
|