ENST00000695651.1:n.1141C>G
|
|
|
ENST00000695652.1:c.2670C>G
|
ENSP00000512083.1:p.Val890=
|
|
ENST00000695653.1:c.702C>G
|
ENSP00000512084.1:p.Val234=
|
|
ENST00000695654.1:c.1917C>G
|
ENSP00000512085.1:p.Val639=
|
|
ENST00000695655.1:c.1734C>G
|
ENSP00000512086.1:n.1734C>G
|
|
ENST00000695692.1:n.2157C>G
|
|
|
ENST00000245907.11:c.2793C>G
MANE Select
|
ENSP00000245907.4:p.Val931=
|
|
ENST00000245907.10:c.2793C>G
|
ENSP00000245907.4:p.Val931=
|
|
ENST00000594005.1:n.369C>G
|
|
|
NM_000064.3:c.2793C>G
|
NP_000055.2:p.Val931=
|
|
NM_000064.4:c.2793C>G
MANE Select
|
NP_000055.2:p.Val931=
|
|