|
NM_006767.4:c.2187C>T
MANE Select
|
NP_006758.2:p.Tyr729=
|
|
ENST00000646124.2:c.2187C>T
MANE Select
|
ENSP00000496779.1:p.Tyr729=
|
|
NM_006767.3:c.2187C>T
|
NP_006758.2:p.Tyr729=
|
|
ENST00000215739.12:c.2187C>T
|
ENSP00000215739.8:p.Tyr729=
|
|
ENST00000415354.6:c.616C>T
|
ENSP00000393765.2:n.616C>T
|
|
ENST00000415817.1:c.85C>T
|
|
|
ENST00000415817.2:c.616C>T
|
|
|
ENST00000439171.5:c.586C>T
|
|
|
ENST00000452988.5:c.349C>T
|
ENSP00000408789.1:n.349C>T
|
|
ENST00000463909.1:n.902C>T
|
|
|
ENST00000479606.5:n.2333C>T
|
|
|
ENST00000495142.6:n.2539C>T
|
|
|
ENST00000498649.1:n.203C>T
|
|
|
ENST00000642151.1:c.2018C>T
|
|
|
ENST00000643578.1:n.2209C>T
|
|
|
ENST00000643710.1:n.1048C>T
|
|
|
ENST00000646506.1:n.2054C>T
|
|
|
ENST00000700578.1:c.2187C>T
|
ENSP00000515073.1:p.Tyr729=
|