ENST00000695651.1:n.2852C>T
|
|
|
ENST00000695653.1:c.2413C>T
|
ENSP00000512084.1:p.Leu805=
|
|
ENST00000695654.1:c.3529C>T
|
ENSP00000512085.1:p.Leu1177=
|
|
ENST00000695689.1:c.475C>T
|
ENSP00000512101.1:n.475C>T
|
|
ENST00000695690.1:n.1569C>T
|
|
|
ENST00000695691.1:n.1365C>T
|
|
|
ENST00000245907.11:c.4504C>T
MANE Select
|
ENSP00000245907.4:p.Leu1502=
|
|
ENST00000245907.10:c.4504C>T
|
ENSP00000245907.4:p.Leu1502=
|
|
ENST00000599668.1:n.99C>T
|
|
|
ENST00000599899.5:n.1463C>T
|
|
|
ENST00000601008.1:c.242-1491C>T
|
ENSP00000471384.1:n.242-1491C>T
|
|
NM_000064.3:c.4504C>T
|
NP_000055.2:p.Leu1502=
|
|
NM_000064.4:c.4504C>T
MANE Select
|
NP_000055.2:p.Leu1502=
|
|