ENST00000695651.1:n.865T=
|
|
|
ENST00000695652.1:c.2394T=
|
ENSP00000512083.1:p.Val798=
|
|
ENST00000695653.1:c.426T=
|
ENSP00000512084.1:p.Val142=
|
|
ENST00000695654.1:c.1641T=
|
ENSP00000512085.1:p.Val547=
|
|
ENST00000695655.1:c.1458T=
|
ENSP00000512086.1:n.1458T=
|
|
ENST00000695692.1:n.1881T=
|
|
|
ENST00000245907.11:c.2517T=
MANE Select
|
ENSP00000245907.4:p.Val839=
|
|
ENST00000245907.10:c.2517T=
|
ENSP00000245907.4:p.Val839=
|
|
ENST00000602053.1:n.565T=
|
|
|
NM_000064.3:c.2517T=
|
NP_000055.2:p.Val839=
|
|
NM_000064.4:c.2517T=
MANE Select
|
NP_000055.2:p.Val839=
|
|