ENST00000452035.7:n.298G=
|
|
|
ENST00000483004.2:c.121G=
|
ENSP00000419887.2:p.Gly41=
|
|
ENST00000497841.6:c.121G=
|
ENSP00000513847.1:p.Gly41=
|
|
ENST00000698628.1:c.121G=
|
ENSP00000513848.1:p.Gly41=
|
|
ENST00000698629.1:n.298G=
|
|
|
ENST00000698630.1:n.282G=
|
|
|
ENST00000698631.1:n.277G=
|
|
|
ENST00000698632.1:n.249G=
|
|
|
ENST00000698633.1:n.219G=
|
|
|
ENST00000698636.1:n.343G=
|
|
|
ENST00000425368.7:c.121G=
MANE Select
|
ENSP00000416561.2:p.Gly41=
|
|
ENST00000425368.6:c.121G=
|
ENSP00000416561.2:p.Gly41=
|
|
ENST00000452035.6:n.121G=
|
|
|
ENST00000456570.5:c.1627G=
|
ENSP00000410815.1:p.Gly543=
|
|
ENST00000460718.5:c.65-57G=
|
ENSP00000417793.1:n.65-57G=
|
|
ENST00000472581.1:n.368G=
|
|
|
ENST00000475617.5:c.121G=
|
ENSP00000420090.1:p.Gly41=
|
|
ENST00000477310.1:c.1352-578G=
|
ENSP00000418996.1:n.1352-578G=
|
|
NM_001710.5:c.121G= , LRG_136t1:c.121G=
|
NP_001701.2:p.Gly41=
|
|
NM_001710.6:c.121G=
MANE Select
|
NP_001701.2:p.Gly41=
|
|