ENST00000695651.1:n.811C>T
|
|
|
ENST00000695652.1:c.2340C>T
|
ENSP00000512083.1:p.Phe780=
|
|
ENST00000695653.1:c.372C>T
|
ENSP00000512084.1:p.Phe124=
|
|
ENST00000695654.1:c.1587C>T
|
ENSP00000512085.1:p.Phe529=
|
|
ENST00000695655.1:c.1404C>T
|
ENSP00000512086.1:n.1404C>T
|
|
ENST00000695692.1:n.1827C>T
|
|
|
ENST00000245907.11:c.2463C>T
MANE Select
|
ENSP00000245907.4:p.Phe821=
|
|
ENST00000245907.10:c.2463C>T
|
ENSP00000245907.4:p.Phe821=
|
|
ENST00000602053.1:n.511C>T
|
|
|
NM_000064.3:c.2463C>T
|
NP_000055.2:p.Phe821=
|
|
NM_000064.4:c.2463C>T
MANE Select
|
NP_000055.2:p.Phe821=
|
|