ENST00000695651.1:n.2645G>A
|
|
|
ENST00000695653.1:c.2206G>A
|
ENSP00000512084.1:p.Glu736Lys
|
|
ENST00000695654.1:c.3322G>A
|
ENSP00000512085.1:p.Glu1108Lys
|
|
ENST00000695689.1:c.268G>A
|
ENSP00000512101.1:n.268G>A
|
|
ENST00000695690.1:n.488G>A
|
|
|
ENST00000695691.1:n.488G>A
|
|
|
ENST00000245907.11:c.4297G>A
MANE Select
|
ENSP00000245907.4:p.Glu1433Lys
|
|
ENST00000245907.10:c.4297G>A
|
ENSP00000245907.4:p.Glu1433Lys
|
|
ENST00000596548.1:c.418G>A
|
ENSP00000469744.1:p.Glu140Lys
|
|
ENST00000599899.5:n.1256G>A
|
|
|
ENST00000601008.1:c.242-4036G>A
|
ENSP00000471384.1:n.242-4036G>A
|
|
NM_000064.3:c.4297G>A
|
NP_000055.2:p.Glu1433Lys
|
|
NM_000064.4:c.4297G>A
MANE Select
|
NP_000055.2:p.Glu1433Lys
|
|