ENST00000703783.1:n.1103T>A
|
|
|
ENST00000703785.1:n.1184T>A
|
|
|
ENST00000262464.9:c.4319T>A
MANE Select
|
ENSP00000262464.4:p.Phe1440Tyr
|
|
ENST00000262464.8:c.4319T>A
|
ENSP00000262464.4:p.Phe1440Tyr
|
|
ENST00000507835.5:c.869T>A
|
ENSP00000426839.1:p.Phe290Tyr
|
|
ENST00000508053.5:c.4319T>A
|
ENSP00000424571.1:p.Phe1440Tyr
|
|
ENST00000508989.5:c.4220T>A
|
ENSP00000425596.1:p.Phe1407Tyr
|
|
ENST00000619499.4:c.4316T>A
|
ENSP00000482132.1:p.Phe1439Tyr
|
|
NM_001999.3:c.4319T>A
|
NP_001990.2:p.Phe1440Tyr
|
|
XM_017009228.2:c.4166T>A
|
XP_016864717.1:p.Phe1389Tyr
|
|
NM_001999.4:c.4319T>A
MANE Select
|
NP_001990.2:p.Phe1440Tyr
|
|