ENST00000695651.1:n.1096C>G
|
|
|
ENST00000695652.1:c.2625C>G
|
ENSP00000512083.1:p.Val875=
|
|
ENST00000695653.1:c.657C>G
|
ENSP00000512084.1:p.Val219=
|
|
ENST00000695654.1:c.1872C>G
|
ENSP00000512085.1:p.Val624=
|
|
ENST00000695655.1:c.1689C>G
|
ENSP00000512086.1:n.1689C>G
|
|
ENST00000695692.1:n.2112C>G
|
|
|
ENST00000245907.11:c.2748C>G
MANE Select
|
ENSP00000245907.4:p.Val916=
|
|
ENST00000245907.10:c.2748C>G
|
ENSP00000245907.4:p.Val916=
|
|
ENST00000594005.1:n.324C>G
|
|
|
NM_000064.3:c.2748C>G
|
NP_000055.2:p.Val916=
|
|
NM_000064.4:c.2748C>G
MANE Select
|
NP_000055.2:p.Val916=
|
|