|
NM_006767.4:c.1794C>A
MANE Select
|
NP_006758.2:p.Cys598Ter
|
|
ENST00000646124.2:c.1794C>A
MANE Select
|
ENSP00000496779.1:p.Cys598Ter
|
|
NM_006767.3:c.1794C>A
|
NP_006758.2:p.Cys598Ter
|
|
ENST00000215739.12:c.1794C>A
|
ENSP00000215739.8:p.Cys598Ter
|
|
ENST00000415354.6:c.106C>A
|
ENSP00000393765.2:p.Pro36Thr
|
|
ENST00000415817.2:c.143-37C>A
|
|
|
ENST00000439171.5:c.76C>A
|
|
|
ENST00000464807.1:n.55C>A
|
|
|
ENST00000479606.5:n.1940C>A
|
|
|
ENST00000491432.5:n.252-37C>A
|
|
|
ENST00000495142.5:n.410C>A
|
|
|
ENST00000495142.6:n.1427C>A
|
|
|
ENST00000642151.1:c.1625C>A
|
|
|
ENST00000643578.1:n.1816C>A
|
|
|
ENST00000643710.1:n.655C>A
|
|
|
ENST00000646506.1:n.1661C>A
|
|
|
ENST00000700578.1:c.1794C>A
|
ENSP00000515073.1:p.Cys598Ter
|