ENST00000467236.2:n.474C>A
|
|
|
ENST00000699980.1:n.1238C>A
|
|
|
ENST00000369980.8:c.1694C>A
MANE Select
|
ENSP00000358997.3:p.Ala565Glu
|
|
ENST00000369973.7:c.*637C>A
|
ENSP00000358990.3:n.*637C>A
|
|
ENST00000369974.6:c.1457C>A
|
ENSP00000358991.2:p.Ala486Glu
|
|
ENST00000369980.7:c.1694C>A
|
ENSP00000358997.3:p.Ala565Glu
|
|
ENST00000393687.6:c.1604C>A
|
ENSP00000377291.2:p.Ala535Glu
|
|
ENST00000429936.6:c.1682C>A
|
ENSP00000392662.2:p.Ala561Glu
|
|
ENST00000437278.5:c.385C>A
|
|
|
ENST00000443220.1:c.939C>A
|
|
|
ENST00000444230.5:c.529-2163C>A
|
ENSP00000399974.1:n.529-2163C>A
|
|
ENST00000444254.1:c.360C>A
|
|
|
ENST00000455690.5:c.280-601C>A
|
ENSP00000411809.1:n.280-601C>A
|
|
ENST00000477274.1:n.616-2468C>A
|
|
|
NM_001025242.1:c.1604C>A
|
NP_001020413.1:p.Ala535Glu
|
|
NM_001025243.1:c.1457C>A
|
NP_001020414.1:p.Ala486Glu
|
|
NM_001569.3:c.1694C>A
|
NP_001560.2:p.Ala565Glu
|
|
XM_005274668.2:c.1682C>A
|
XP_005274725.1:p.Ala561Glu
|
|
XM_011531158.1:c.1367C>A
|
XP_011529460.1:p.Ala456Glu
|
|
XM_005274668.4:c.1682C>A
|
XP_005274725.1:p.Ala561Glu
|
|
NM_001569.4:c.1694C>A
MANE Select
|
NP_001560.2:p.Ala565Glu
|
|
NM_001025242.2:c.1604C>A
|
NP_001020413.1:p.Ala535Glu
|
|
NM_001025243.2:c.1457C>A
|
NP_001020414.1:p.Ala486Glu
|
|