|
NM_006767.4:c.2130C>T
MANE Select
|
NP_006758.2:p.Ile710=
|
|
ENST00000646124.2:c.2130C>T
MANE Select
|
ENSP00000496779.1:p.Ile710=
|
|
NM_006767.3:c.2130C>T
|
NP_006758.2:p.Ile710=
|
|
ENST00000215739.12:c.2130C>T
|
ENSP00000215739.8:p.Ile710=
|
|
ENST00000415354.6:c.559C>T
|
ENSP00000393765.2:n.559C>T
|
|
ENST00000415817.1:c.28C>T
|
|
|
ENST00000415817.2:c.559C>T
|
|
|
ENST00000439171.5:c.529C>T
|
|
|
ENST00000452988.5:c.292C>T
|
ENSP00000408789.1:n.292C>T
|
|
ENST00000463909.1:n.845C>T
|
|
|
ENST00000479606.5:n.2276C>T
|
|
|
ENST00000495142.6:n.2482C>T
|
|
|
ENST00000498649.1:n.146C>T
|
|
|
ENST00000642151.1:c.1961C>T
|
|
|
ENST00000643578.1:n.2152C>T
|
|
|
ENST00000643710.1:n.991C>T
|
|
|
ENST00000646506.1:n.1997C>T
|
|
|
ENST00000700578.1:c.2130C>T
|
ENSP00000515073.1:p.Ile710=
|