ENST00000452035.7:n.2119A>T
|
|
|
ENST00000483004.2:c.1511A>T
|
ENSP00000419887.2:p.Asp504Val
|
|
ENST00000698628.1:c.1624+318A>T
|
ENSP00000513848.1:n.1624+318A>T
|
|
ENST00000698629.1:n.1904A>T
|
|
|
ENST00000698630.1:n.2443A>T
|
|
|
ENST00000698631.1:n.2444A>T
|
|
|
ENST00000698632.1:n.3238A>T
|
|
|
ENST00000698633.1:n.3128A>T
|
|
|
ENST00000698636.1:n.1949A>T
|
|
|
ENST00000425368.7:c.1727A>T
MANE Select
|
ENSP00000416561.2:p.Asp576Val
|
|
ENST00000425368.6:c.1727A>T
|
ENSP00000416561.2:p.Asp576Val
|
|
ENST00000456570.5:c.3233A>T
|
ENSP00000410815.1:p.Asp1078Val
|
|
ENST00000467360.1:n.853A>T
|
|
|
ENST00000477310.1:c.2780A>T
|
ENSP00000418996.1:p.Asp927Val
|
|
ENST00000483004.1:c.349A>T
|
|
|
NM_001710.5:c.1727A>T , LRG_136t1:c.1727A>T
|
NP_001701.2:p.Asp576Val
|
|
NM_001710.6:c.1727A>T
MANE Select
|
NP_001701.2:p.Asp576Val
|
|