|
NM_006767.4:c.2134G>T
MANE Select
|
NP_006758.2:p.Glu712Ter
|
|
ENST00000646124.2:c.2134G>T
MANE Select
|
ENSP00000496779.1:p.Glu712Ter
|
|
NM_006767.3:c.2134G>T
|
NP_006758.2:p.Glu712Ter
|
|
ENST00000215739.12:c.2134G>T
|
ENSP00000215739.8:p.Glu712Ter
|
|
ENST00000415354.6:c.563G>T
|
ENSP00000393765.2:n.563G>T
|
|
ENST00000415817.1:c.32G>T
|
|
|
ENST00000415817.2:c.563G>T
|
|
|
ENST00000439171.5:c.533G>T
|
|
|
ENST00000452988.5:c.296G>T
|
ENSP00000408789.1:n.296G>T
|
|
ENST00000463909.1:n.849G>T
|
|
|
ENST00000479606.5:n.2280G>T
|
|
|
ENST00000495142.6:n.2486G>T
|
|
|
ENST00000498649.1:n.150G>T
|
|
|
ENST00000642151.1:c.1965G>T
|
|
|
ENST00000643578.1:n.2156G>T
|
|
|
ENST00000643710.1:n.995G>T
|
|
|
ENST00000646506.1:n.2001G>T
|
|
|
ENST00000700578.1:c.2134G>T
|
ENSP00000515073.1:p.Glu712Ter
|