ENST00000695651.1:n.793C>T
|
|
|
ENST00000695652.1:c.2322C>T
|
ENSP00000512083.1:p.Ile774=
|
|
ENST00000695653.1:c.354C>T
|
ENSP00000512084.1:p.Ile118=
|
|
ENST00000695654.1:c.1569C>T
|
ENSP00000512085.1:p.Ile523=
|
|
ENST00000695655.1:c.1386C>T
|
ENSP00000512086.1:n.1386C>T
|
|
ENST00000695692.1:n.1809C>T
|
|
|
ENST00000245907.11:c.2445C>T
MANE Select
|
ENSP00000245907.4:p.Ile815=
|
|
ENST00000245907.10:c.2445C>T
|
ENSP00000245907.4:p.Ile815=
|
|
ENST00000602053.1:n.493C>T
|
|
|
NM_000064.3:c.2445C>T
|
NP_000055.2:p.Ile815=
|
|
NM_000064.4:c.2445C>T
MANE Select
|
NP_000055.2:p.Ile815=
|
|