ENST00000396623.8:c.1035A>T
MANE Select
|
ENSP00000379865.3:p.Ala345=
|
|
ENST00000648156.1:c.*254A>T
|
ENSP00000497007.1:n.*254A>T
|
|
ENST00000276576.11:c.*871A>T
|
ENSP00000276576.7:n.*871A>T
|
|
ENST00000396623.7:c.1035A>T
|
ENSP00000379865.3:p.Ala345=
|
|
ENST00000415254.5:c.891A>T
|
ENSP00000407115.1:p.Ala297=
|
|
ENST00000419955.5:c.*1044A>T
|
ENSP00000392040.1:n.*1044A>T
|
|
ENST00000424777.6:c.*472A>T
|
ENSP00000410883.2:n.*472A>T
|
|
ENST00000426810.5:c.*1220A>T
|
ENSP00000406905.1:n.*1220A>T
|
|
ENST00000480040.5:n.110A>T
|
|
|
ENST00000496501.5:n.909A>T
|
|
|
NM_144650.2:c.1035A>T
|
NP_653251.2:p.Ala345=
|
|
NM_144650.3:c.1035A>T
MANE Select
|
NP_653251.2:p.Ala345=
|
|