|
NM_006767.4:c.1729C>T
MANE Select
|
NP_006758.2:p.Gln577Ter
|
|
ENST00000646124.2:c.1729C>T
MANE Select
|
ENSP00000496779.1:p.Gln577Ter
|
|
NM_006767.3:c.1729C>T
|
NP_006758.2:p.Gln577Ter
|
|
ENST00000215739.12:c.1729C>T
|
ENSP00000215739.8:p.Gln577Ter
|
|
ENST00000415354.6:c.44-3C>T
|
ENSP00000393765.2:n.44-3C>T
|
|
ENST00000415817.2:c.86C>T
|
|
|
ENST00000439171.5:c.11C>T
|
|
|
ENST00000479606.5:n.1875C>T
|
|
|
ENST00000491432.5:n.195C>T
|
|
|
ENST00000495142.5:n.345C>T
|
|
|
ENST00000495142.6:n.1362C>T
|
|
|
ENST00000642151.1:c.1560C>T
|
|
|
ENST00000643578.1:n.1751C>T
|
|
|
ENST00000643710.1:n.590C>T
|
|
|
ENST00000646506.1:n.1596C>T
|
|
|
ENST00000700578.1:c.1729C>T
|
ENSP00000515073.1:p.Gln577Ter
|