ENST00000703783.1:n.725T>A
|
|
|
ENST00000703785.1:n.806T>A
|
|
|
ENST00000262464.9:c.3941T>A
MANE Select
|
ENSP00000262464.4:p.Phe1314Tyr
|
|
ENST00000262464.8:c.3941T>A
|
ENSP00000262464.4:p.Phe1314Tyr
|
|
ENST00000507835.5:c.491T>A
|
ENSP00000426839.1:p.Phe164Tyr
|
|
ENST00000508053.5:c.3941T>A
|
ENSP00000424571.1:p.Phe1314Tyr
|
|
ENST00000508989.5:c.3842T>A
|
ENSP00000425596.1:p.Phe1281Tyr
|
|
ENST00000619499.4:c.3938T>A
|
ENSP00000482132.1:p.Phe1313Tyr
|
|
NM_001999.3:c.3941T>A
|
NP_001990.2:p.Phe1314Tyr
|
|
XM_017009228.2:c.3788T>A
|
XP_016864717.1:p.Phe1263Tyr
|
|
NM_001999.4:c.3941T>A
MANE Select
|
NP_001990.2:p.Phe1314Tyr
|
|