|
NM_006767.4:c.2350C>T
MANE Select
|
NP_006758.2:p.Gln784Ter
|
|
ENST00000646124.2:c.2350C>T
MANE Select
|
ENSP00000496779.1:p.Gln784Ter
|
|
NM_006767.3:c.2350C>T
|
NP_006758.2:p.Gln784Ter
|
|
ENST00000215739.12:c.2350C>T
|
ENSP00000215739.8:p.Gln784Ter
|
|
ENST00000415817.1:c.248C>T
|
|
|
ENST00000415817.2:c.779C>T
|
|
|
ENST00000452988.5:c.512C>T
|
ENSP00000408789.1:n.512C>T
|
|
ENST00000463909.1:n.1648C>T
|
|
|
ENST00000479606.5:n.2496C>T
|
|
|
ENST00000495142.6:n.2702C>T
|
|
|
ENST00000498649.1:n.450C>T
|
|
|
ENST00000642151.1:c.2181C>T
|
|
|
ENST00000643578.1:n.2372C>T
|
|
|
ENST00000643710.1:n.1211C>T
|
|
|
ENST00000646506.1:n.2217C>T
|
|
|
ENST00000700578.1:c.2325+109C>T
|
ENSP00000515073.1:n.2325+109C>T
|