|
NM_006767.4:c.844C>T
MANE Select
|
NP_006758.2:p.Gln282Ter
|
|
ENST00000646124.2:c.844C>T
MANE Select
|
ENSP00000496779.1:p.Gln282Ter
|
|
NM_006767.3:c.844C>T
|
NP_006758.2:p.Gln282Ter
|
|
ENST00000215739.12:c.844C>T
|
ENSP00000215739.8:p.Gln282Ter
|
|
ENST00000414985.5:c.*410C>T
|
ENSP00000397247.1:n.*410C>T
|
|
ENST00000479606.5:n.990C>T
|
|
|
ENST00000495142.6:n.189C>T
|
|
|
ENST00000497716.5:n.671C>T
|
|
|
ENST00000642151.1:c.675C>T
|
|
|
ENST00000643578.1:n.866C>T
|
|
|
ENST00000646506.1:n.423C>T
|
|
|
ENST00000700578.1:c.844C>T
|
ENSP00000515073.1:p.Gln282Ter
|