ENST00000695651.1:n.2534C=
|
|
|
ENST00000695653.1:c.2095C=
|
ENSP00000512084.1:p.Gln699=
|
|
ENST00000695654.1:c.3211C=
|
ENSP00000512085.1:p.Gln1071=
|
|
ENST00000695689.1:c.157C=
|
ENSP00000512101.1:n.157C=
|
|
ENST00000695690.1:n.377C=
|
|
|
ENST00000695691.1:n.377C=
|
|
|
ENST00000245907.11:c.4186C=
MANE Select
|
ENSP00000245907.4:p.Gln1396=
|
|
ENST00000245907.10:c.4186C=
|
ENSP00000245907.4:p.Gln1396=
|
|
ENST00000596548.1:c.307C=
|
ENSP00000469744.1:p.Gln103=
|
|
ENST00000599899.5:n.1145C=
|
|
|
ENST00000601008.1:c.242-4258C=
|
ENSP00000471384.1:n.242-4258C=
|
|
NM_000064.3:c.4186C=
|
NP_000055.2:p.Gln1396=
|
|
NM_000064.4:c.4186C=
MANE Select
|
NP_000055.2:p.Gln1396=
|
|