ENST00000695651.1:n.2626C=
|
|
|
ENST00000695653.1:c.2187C=
|
ENSP00000512084.1:p.Asp729=
|
|
ENST00000695654.1:c.3303C=
|
ENSP00000512085.1:p.Asp1101=
|
|
ENST00000695689.1:c.249C=
|
ENSP00000512101.1:n.249C=
|
|
ENST00000695690.1:n.469C=
|
|
|
ENST00000695691.1:n.469C=
|
|
|
ENST00000245907.11:c.4278C=
MANE Select
|
ENSP00000245907.4:p.Asp1426=
|
|
ENST00000245907.10:c.4278C=
|
ENSP00000245907.4:p.Asp1426=
|
|
ENST00000596548.1:c.399C=
|
ENSP00000469744.1:p.Asp133=
|
|
ENST00000599899.5:n.1237C=
|
|
|
ENST00000601008.1:c.242-4055C=
|
ENSP00000471384.1:n.242-4055C=
|
|
NM_000064.3:c.4278C=
|
NP_000055.2:p.Asp1426=
|
|
NM_000064.4:c.4278C=
MANE Select
|
NP_000055.2:p.Asp1426=
|
|