ENST00000700578.1:c.848G>A
|
ENSP00000515073.1:p.Arg283Gln
|
|
ENST00000495142.6:n.193G>A
|
|
|
ENST00000642151.1:c.679G>A
|
|
|
ENST00000643578.1:n.870G>A
|
|
|
ENST00000646124.2:c.848G>A
MANE Select
|
ENSP00000496779.1:p.Arg283Gln
|
|
ENST00000646506.1:n.427G>A
|
|
|
ENST00000215739.12:c.848G>A
|
ENSP00000215739.8:p.Arg283Gln
|
|
ENST00000414985.5:c.*414G>A
|
ENSP00000397247.1:n.*414G>A
|
|
ENST00000479606.5:n.994G>A
|
|
|
ENST00000497716.5:n.675G>A
|
|
|
NM_006767.3:c.848G>A
|
NP_006758.2:p.Arg283Gln
|
|
NM_006767.4:c.848G>A
MANE Select
|
NP_006758.2:p.Arg283Gln
|
|