NM_007055.4:c.1930G=
MANE Select
|
NP_008986.2:p.Glu644=
|
ENST00000372371.8:c.1930G=
MANE Select
|
ENSP00000361446.3:p.Glu644=
|
NM_007055.3:c.1930G=
|
NP_008986.2:p.Glu644=
|
ENST00000372371.7:c.1930G=
|
ENSP00000361446.3:p.Glu644=
|
ENST00000472014.5:n.152G=
|
|
ENST00000473588.2:c.593G=
|
|
ENST00000698727.1:n.990G=
|
|
ENST00000698728.1:n.1509G=
|
|
ENST00000698729.1:n.3055G=
|
|
ENST00000698730.1:n.3055G=
|
|
ENST00000698731.1:c.1789G=
|
ENSP00000513898.1:p.Glu597=
|
ENST00000698732.1:c.*791G=
|
ENSP00000513899.1:n.*791G=
|
ENST00000698733.1:c.*1117G=
|
ENSP00000513900.1:n.*1117G=
|
ENST00000698734.1:c.1930G=
|
ENSP00000513901.1:p.Glu644=
|
ENST00000698735.1:n.2045G=
|
|
ENST00000698736.1:n.2045G=
|
|
ENST00000698737.1:n.2045G=
|
|
ENST00000698738.1:n.2045G=
|
|
ENST00000698739.1:n.2045G=
|
|