ENST00000470094.2:c.*341T>A
|
ENSP00000434898.2:n.*341T>A
|
|
ENST00000528762.2:c.*1185T>A
|
ENSP00000433168.2:n.*1185T>A
|
|
ENST00000530893.7:c.9449T>A
|
ENSP00000499438.2:p.Phe3150Tyr
|
|
ENST00000665585.2:c.*1380T>A
|
ENSP00000499570.2:n.*1380T>A
|
|
ENST00000700202.2:c.9767T>A
|
ENSP00000514856.2:p.Phe3256Tyr
|
|
ENST00000700202.1:c.2234T>A
|
ENSP00000514856.1:p.Phe745Tyr
|
|
ENST00000700203.1:n.1945T>A
|
|
|
ENST00000380152.8:c.9818T>A
MANE Select
|
ENSP00000369497.3:p.Phe3273Tyr
|
|
ENST00000544455.6:c.9818T>A
|
ENSP00000439902.1:p.Phe3273Tyr
|
|
ENST00000614259.2:c.9826T>A
|
ENSP00000506251.1:n.9826T>A
|
|
ENST00000680887.1:c.9818T>A
|
ENSP00000505508.1:p.Phe3273Tyr
|
|
ENST00000380152.7:c.9818T>A
|
ENSP00000369497.3:p.Phe3273Tyr
|
|
ENST00000533776.1:n.406T>A
|
|
|
ENST00000544455.5:c.9818T>A
|
ENSP00000439902.1:p.Phe3273Tyr
|
|
NM_000059.3:c.9818T>A , LRG_293t1:c.9818T>A
|
NP_000050.2:p.Phe3273Tyr
|
|
XM_011535203.1:c.9818T>A
|
XP_011533505.1:p.Phe3273Tyr
|
|
XM_011535204.1:c.9722T>A
|
XP_011533506.1:p.Phe3241Tyr
|
|
NM_000059.4:c.9818T>A
MANE Select
|
NP_000050.3:p.Phe3273Tyr
|
|