ENST00000452035.7:n.2023A>T
|
|
|
ENST00000483004.2:c.1415A>T
|
ENSP00000419887.2:p.Glu472Val
|
|
ENST00000698628.1:c.1624+222A>T
|
ENSP00000513848.1:n.1624+222A>T
|
|
ENST00000698629.1:n.1808A>T
|
|
|
ENST00000698630.1:n.2347A>T
|
|
|
ENST00000698631.1:n.2348A>T
|
|
|
ENST00000698632.1:n.3142A>T
|
|
|
ENST00000698633.1:n.3032A>T
|
|
|
ENST00000698636.1:n.1853A>T
|
|
|
ENST00000425368.7:c.1631A>T
MANE Select
|
ENSP00000416561.2:p.Glu544Val
|
|
ENST00000425368.6:c.1631A>T
|
ENSP00000416561.2:p.Glu544Val
|
|
ENST00000452035.6:n.1846A>T
|
|
|
ENST00000456570.5:c.3137A>T
|
ENSP00000410815.1:p.Glu1046Val
|
|
ENST00000467360.1:n.757A>T
|
|
|
ENST00000477310.1:c.2684A>T
|
ENSP00000418996.1:p.Glu895Val
|
|
ENST00000483004.1:c.253A>T
|
|
|
NM_001710.5:c.1631A>T , LRG_136t1:c.1631A>T
|
NP_001701.2:p.Glu544Val
|
|
NM_001710.6:c.1631A>T
MANE Select
|
NP_001701.2:p.Glu544Val
|
|