ENST00000695651.1:n.833T>A
|
|
|
ENST00000695652.1:c.2362T>A
|
ENSP00000512083.1:p.Phe788Ile
|
|
ENST00000695653.1:c.394T>A
|
ENSP00000512084.1:p.Phe132Ile
|
|
ENST00000695654.1:c.1609T>A
|
ENSP00000512085.1:p.Phe537Ile
|
|
ENST00000695655.1:c.1426T>A
|
ENSP00000512086.1:n.1426T>A
|
|
ENST00000695692.1:n.1849T>A
|
|
|
ENST00000245907.11:c.2485T>A
MANE Select
|
ENSP00000245907.4:p.Phe829Ile
|
|
ENST00000245907.10:c.2485T>A
|
ENSP00000245907.4:p.Phe829Ile
|
|
ENST00000602053.1:n.533T>A
|
|
|
NM_000064.3:c.2485T>A
|
NP_000055.2:p.Phe829Ile
|
|
NM_000064.4:c.2485T>A
MANE Select
|
NP_000055.2:p.Phe829Ile
|
|