ENST00000452035.7:n.2290G=
|
|
|
ENST00000483004.2:c.1587G=
|
ENSP00000419887.2:p.Glu529=
|
|
ENST00000698628.1:c.1625-252G=
|
ENSP00000513848.1:n.1625-252G=
|
|
ENST00000698629.1:n.2075G=
|
|
|
ENST00000698630.1:n.2519G=
|
|
|
ENST00000698631.1:n.2520G=
|
|
|
ENST00000698632.1:n.3409G=
|
|
|
ENST00000698633.1:n.3299G=
|
|
|
ENST00000425368.7:c.1803G=
MANE Select
|
ENSP00000416561.2:p.Glu601=
|
|
ENST00000425368.6:c.1803G=
|
ENSP00000416561.2:p.Glu601=
|
|
ENST00000456570.5:c.3309G=
|
ENSP00000410815.1:p.Glu1103=
|
|
ENST00000467360.1:n.929G=
|
|
|
ENST00000477310.1:c.2856G=
|
ENSP00000418996.1:p.Glu952=
|
|
ENST00000482312.1:n.19G=
|
|
|
ENST00000483004.1:c.425G=
|
|
|
NM_001710.5:c.1803G= , LRG_136t1:c.1803G=
|
NP_001701.2:p.Glu601=
|
|
NM_001710.6:c.1803G=
MANE Select
|
NP_001701.2:p.Glu601=
|
|