ENST00000625662.3:c.2126A>T
|
|
|
ENST00000628118.2:c.1653A>T
|
|
|
ENST00000700551.1:c.*1450A>T
|
ENSP00000515057.1:n.*1450A>T
|
|
ENST00000394196.9:c.2619A>T
MANE Select
|
ENSP00000377747.4:p.Gly873=
|
|
ENST00000635856.1:n.3191A>T
|
|
|
ENST00000636306.1:n.179A>T
|
|
|
ENST00000636881.1:c.1990A>T
|
|
|
ENST00000637572.1:n.3363A>T
|
|
|
ENST00000394196.8:c.2619A>T
|
ENSP00000377747.4:p.Gly873=
|
|
ENST00000625463.1:c.159A>T
|
ENSP00000486391.1:p.Gly53=
|
|
ENST00000626874.2:c.2619A>T
|
ENSP00000486629.1:p.Gly873=
|
|
ENST00000628118.1:n.398A>T
|
|
|
NM_001271.3:c.2619A>T
|
NP_001262.3:p.Gly873=
|
|
NM_001271.4:c.2619A>T
MANE Select
|
NP_001262.3:p.Gly873=
|
|