ENST00000698724.1:n.10A>T
|
|
|
ENST00000698727.1:n.1802A>T
|
|
|
ENST00000698728.1:n.2321A>T
|
|
|
ENST00000698729.1:n.3867A>T
|
|
|
ENST00000698730.1:n.3867A>T
|
|
|
ENST00000698731.1:c.2601A>T
|
ENSP00000513898.1:p.Gly867=
|
|
ENST00000698732.1:c.*1603A>T
|
ENSP00000513899.1:n.*1603A>T
|
|
ENST00000698733.1:c.*1929A>T
|
ENSP00000513900.1:n.*1929A>T
|
|
ENST00000698734.1:c.*266A>T
|
ENSP00000513901.1:n.*266A>T
|
|
ENST00000698735.1:n.2857A>T
|
|
|
ENST00000698736.1:n.2857A>T
|
|
|
ENST00000698737.1:n.2857A>T
|
|
|
ENST00000698738.1:n.2857A>T
|
|
|
ENST00000698739.1:n.2857A>T
|
|
|
ENST00000372371.8:c.2742A>T
MANE Select
|
ENSP00000361446.3:p.Gly914=
|
|
ENST00000372371.7:c.2742A>T
|
ENSP00000361446.3:p.Gly914=
|
|
ENST00000472014.5:n.595A>T
|
|
|
NM_007055.3:c.2742A>T
|
NP_008986.2:p.Gly914=
|
|
NM_007055.4:c.2742A>T
MANE Select
|
NP_008986.2:p.Gly914=
|
|