ENST00000452035.7:n.2090A>C
|
|
|
ENST00000483004.2:c.1482A>C
|
ENSP00000419887.2:p.Glu494Asp
|
|
ENST00000698628.1:c.1624+289A>C
|
ENSP00000513848.1:n.1624+289A>C
|
|
ENST00000698629.1:n.1875A>C
|
|
|
ENST00000698630.1:n.2414A>C
|
|
|
ENST00000698631.1:n.2415A>C
|
|
|
ENST00000698632.1:n.3209A>C
|
|
|
ENST00000698633.1:n.3099A>C
|
|
|
ENST00000698636.1:n.1920A>C
|
|
|
ENST00000425368.7:c.1698A>C
MANE Select
|
ENSP00000416561.2:p.Glu566Asp
|
|
ENST00000425368.6:c.1698A>C
|
ENSP00000416561.2:p.Glu566Asp
|
|
ENST00000456570.5:c.3204A>C
|
ENSP00000410815.1:p.Glu1068Asp
|
|
ENST00000467360.1:n.824A>C
|
|
|
ENST00000477310.1:c.2751A>C
|
ENSP00000418996.1:p.Glu917Asp
|
|
ENST00000483004.1:c.320A>C
|
|
|
NM_001710.5:c.1698A>C , LRG_136t1:c.1698A>C
|
NP_001701.2:p.Glu566Asp
|
|
NM_001710.6:c.1698A>C
MANE Select
|
NP_001701.2:p.Glu566Asp
|
|