ENST00000426304.6:c.545A>T
|
ENSP00000394896.2:p.Glu182Val
|
|
ENST00000457600.3:c.545A>T
|
ENSP00000407201.2:p.Glu182Val
|
|
ENST00000698174.1:c.545A>T
|
ENSP00000513594.1:p.Glu182Val
|
|
ENST00000698175.1:c.*292A>T
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ENSP00000513595.1:n.*292A>T
|
|
ENST00000698176.1:n.617A>T
|
|
|
ENST00000698202.1:c.545A>T
|
ENSP00000513605.1:p.Glu182Val
|
|
ENST00000698203.1:c.545A>T
|
ENSP00000513606.1:p.Glu182Val
|
|
ENST00000356853.10:c.545A>T
MANE Select
|
ENSP00000349313.5:p.Glu182Val
|
|
ENST00000318673.6:c.*1667A>T
|
ENSP00000320919.3:n.*1667A>T
|
|
ENST00000356853.9:c.545A>T
|
ENSP00000349313.5:p.Glu182Val
|
|
ENST00000409720.5:c.545A>T
|
ENSP00000387290.1:p.Glu182Val
|
|
ENST00000418099.5:c.545A>T
|
ENSP00000408966.1:p.Glu182Val
|
|
ENST00000426304.5:c.305A>T
|
ENSP00000394896.1:p.Glu102Val
|
|
ENST00000450447.1:c.*232A>T
|
ENSP00000408421.1:n.*232A>T
|
|
ENST00000457600.2:c.545A>T
|
ENSP00000407201.1:p.Glu182Val
|
|
ENST00000498327.5:n.2733A>T
|
|
|
NM_024782.2:c.545A>T , LRG_90t1:c.545A>T
|
NP_079058.1:p.Glu182Val
|
|
NM_001377498.1:c.545A>T
|
NP_001364427.1:p.Glu182Val
|
|
NM_001377499.1:c.545A>T
|
NP_001364428.1:p.Glu182Val
|
|
NM_024782.3:c.545A>T
MANE Select
|
NP_079058.1:p.Glu182Val
|
|
NR_165304.1:n.641A>T
|
|
|