ENST00000307363.10:c.1216T>A
MANE Select
|
ENSP00000306920.4:p.Phe406Ile
|
|
ENST00000307363.9:c.1216T>A
|
ENSP00000306920.4:p.Phe406Ile
|
|
ENST00000307377.12:c.823T>A
|
ENSP00000305920.8:p.Phe275Ile
|
|
ENST00000399402.7:c.1126T>A
|
ENSP00000382333.2:p.Phe376Ile
|
|
ENST00000461475.5:n.315T>A
|
|
|
ENST00000467571.5:n.253T>A
|
|
|
ENST00000473477.1:n.248T>A
|
|
|
ENST00000497796.5:n.468T>A
|
|
|
NM_000404.2:c.1216T>A
|
NP_000395.2:p.Phe406Ile
|
|
NM_000404.3:c.1216T>A
|
NP_000395.2:p.Phe406Ile
|
|
NM_001079811.1:c.1126T>A
|
NP_001073279.1:p.Phe376Ile
|
|
NM_001079811.2:c.1126T>A
|
NP_001073279.1:p.Phe376Ile
|
|
NM_001135602.1:c.823T>A
|
NP_001129074.1:p.Phe275Ile
|
|
NM_001135602.2:c.823T>A
|
NP_001129074.1:p.Phe275Ile
|
|
NM_001317040.1:c.1360T>A
|
NP_001303969.1:p.Phe454Ile
|
|
XR_001740634.1:n.1543-605A>T
|
|
|
NM_000404.4:c.1216T>A
MANE Select
|
NP_000395.3:p.Phe406Ile
|
|
NM_001079811.3:c.1126T>A
|
NP_001073279.2:p.Phe376Ile
|
|
NM_001135602.3:c.823T>A
|
NP_001129074.2:p.Phe275Ile
|
|
NM_001317040.2:c.1360T>A
|
NP_001303969.2:p.Phe454Ile
|
|
NM_001393580.1:c.1216T>A
|
NP_001380509.1:p.Phe406Ile
|
|