|
NM_006767.4:c.2284C>T
MANE Select
|
NP_006758.2:p.Gln762Ter
|
|
ENST00000646124.2:c.2284C>T
MANE Select
|
ENSP00000496779.1:p.Gln762Ter
|
|
NM_006767.3:c.2284C>T
|
NP_006758.2:p.Gln762Ter
|
|
ENST00000215739.12:c.2284C>T
|
ENSP00000215739.8:p.Gln762Ter
|
|
ENST00000415817.1:c.182C>T
|
|
|
ENST00000415817.2:c.713C>T
|
|
|
ENST00000452988.5:c.446C>T
|
ENSP00000408789.1:n.446C>T
|
|
ENST00000463909.1:n.1582C>T
|
|
|
ENST00000479606.5:n.2430C>T
|
|
|
ENST00000495142.6:n.2636C>T
|
|
|
ENST00000498649.1:n.300C>T
|
|
|
ENST00000642151.1:c.2115C>T
|
|
|
ENST00000643578.1:n.2306C>T
|
|
|
ENST00000643710.1:n.1145C>T
|
|
|
ENST00000646506.1:n.2151C>T
|
|
|
ENST00000700578.1:c.2284C>T
|
ENSP00000515073.1:p.Gln762Ter
|