ENST00000695651.1:n.2533C>T
|
|
|
ENST00000695653.1:c.2094C>T
|
ENSP00000512084.1:p.Asp698=
|
|
ENST00000695654.1:c.3210C>T
|
ENSP00000512085.1:p.Asp1070=
|
|
ENST00000695689.1:c.156C>T
|
ENSP00000512101.1:n.156C>T
|
|
ENST00000695690.1:n.376C>T
|
|
|
ENST00000695691.1:n.376C>T
|
|
|
ENST00000245907.11:c.4185C>T
MANE Select
|
ENSP00000245907.4:p.Asp1395=
|
|
ENST00000245907.10:c.4185C>T
|
ENSP00000245907.4:p.Asp1395=
|
|
ENST00000596548.1:c.306C>T
|
ENSP00000469744.1:p.Asp102=
|
|
ENST00000599899.5:n.1144C>T
|
|
|
ENST00000601008.1:c.242-4259C>T
|
ENSP00000471384.1:n.242-4259C>T
|
|
NM_000064.3:c.4185C>T
|
NP_000055.2:p.Asp1395=
|
|
NM_000064.4:c.4185C>T
MANE Select
|
NP_000055.2:p.Asp1395=
|
|