ENST00000695651.1:n.2090T>A
|
|
|
ENST00000695652.1:c.3619T>A
|
ENSP00000512083.1:p.Phe1207Ile
|
|
ENST00000695653.1:c.1651T>A
|
ENSP00000512084.1:p.Phe551Ile
|
|
ENST00000695654.1:c.2767T>A
|
ENSP00000512085.1:p.Phe923Ile
|
|
ENST00000695655.1:c.2683T>A
|
ENSP00000512086.1:n.2683T>A
|
|
ENST00000695692.1:n.3106T>A
|
|
|
ENST00000245907.11:c.3742T>A
MANE Select
|
ENSP00000245907.4:p.Phe1248Ile
|
|
ENST00000245907.10:c.3742T>A
|
ENSP00000245907.4:p.Phe1248Ile
|
|
ENST00000596238.1:n.185T>A
|
|
|
ENST00000601008.1:c.241+554T>A
|
ENSP00000471384.1:n.241+554T>A
|
|
NM_000064.3:c.3742T>A
|
NP_000055.2:p.Phe1248Ile
|
|
NM_000064.4:c.3742T>A
MANE Select
|
NP_000055.2:p.Phe1248Ile
|
|