|
NM_006767.4:c.2511C>T
MANE Select
|
NP_006758.2:p.Gly837=
|
|
ENST00000646124.2:c.2511C>T
MANE Select
|
ENSP00000496779.1:p.Gly837=
|
|
NM_006767.3:c.2511C>T
|
NP_006758.2:p.Gly837=
|
|
ENST00000215739.12:c.2511C>T
|
ENSP00000215739.8:p.Gly837=
|
|
ENST00000415817.1:c.674C>T
|
|
|
ENST00000415817.2:c.940C>T
|
|
|
ENST00000452988.5:c.673C>T
|
ENSP00000408789.1:n.673C>T
|
|
ENST00000463909.1:n.1809C>T
|
|
|
ENST00000479606.5:n.2657C>T
|
|
|
ENST00000495142.6:n.2863C>T
|
|
|
ENST00000498649.1:n.611C>T
|
|
|
ENST00000642151.1:c.2342C>T
|
|
|
ENST00000643578.1:n.2533C>T
|
|
|
ENST00000643710.1:n.1372C>T
|
|
|
ENST00000646506.1:n.2378C>T
|
|
|
ENST00000700578.1:c.2430C>T
|
ENSP00000515073.1:p.Gly810=
|