ENST00000249806.11:c.713T>A
MANE Select
|
ENSP00000249806.5:p.Phe238Tyr
|
|
ENST00000562767.2:c.84-10735T>A
|
ENSP00000456336.1:n.84-10735T>A
|
|
ENST00000563917.2:n.555T>A
|
|
|
ENST00000565471.6:c.254T>A
|
ENSP00000457384.1:p.Phe85Tyr
|
|
ENST00000635747.1:c.*616T>A
|
ENSP00000490627.1:n.*616T>A
|
|
ENST00000636212.1:c.*383T>A
|
ENSP00000489851.1:n.*383T>A
|
|
ENST00000636674.1:n.1815T>A
|
|
|
ENST00000636964.1:n.2241T>A
|
|
|
ENST00000637054.1:c.198+10173T>A
|
ENSP00000490807.1:n.198+10173T>A
|
|
ENST00000637329.1:c.682T>A
|
|
|
ENST00000637450.1:c.*367T>A
|
ENSP00000490204.1:n.*367T>A
|
|
ENST00000637494.1:c.425T>A
|
ENSP00000490057.1:p.Phe142Tyr
|
|
ENST00000637667.1:c.614T>A
|
ENSP00000489843.1:p.Phe205Tyr
|
|
ENST00000637823.1:c.538T>A
|
|
|
ENST00000637888.1:c.198+10173T>A
|
ENSP00000490546.1:n.198+10173T>A
|
|
ENST00000638076.1:c.*316T>A
|
ENSP00000490373.1:n.*316T>A
|
|
ENST00000638144.1:n.356T>A
|
|
|
ENST00000646164.1:c.39-8682T>A
|
|
|
ENST00000249806.9:c.713T>A
|
ENSP00000249806.5:p.Phe238Tyr
|
|
ENST00000538696.5:c.809T>A
|
ENSP00000445770.1:p.Phe270Tyr
|
|
ENST00000562767.1:c.84-10735T>A
|
ENSP00000456336.1:n.84-10735T>A
|
|
ENST00000564752.1:c.*97T>A
|
ENSP00000457822.1:n.*97T>A
|
|
ENST00000565471.5:c.254T>A
|
ENSP00000457384.1:p.Phe85Tyr
|
|
ENST00000566347.5:c.524T>A
|
ENSP00000457783.1:p.Phe175Tyr
|
|
ENST00000567060.5:c.*111T>A
|
ENSP00000454818.1:n.*111T>A
|
|
NM_017882.2:c.713T>A
|
NP_060352.1:p.Phe238Tyr
|
|
NM_017882.3:c.713T>A
MANE Select
|
NP_060352.1:p.Phe238Tyr
|
|