ENST00000249806.11:c.667T>G
MANE Select
|
ENSP00000249806.5:p.Tyr223Asp
|
|
ENST00000562767.2:c.84-10781T>G
|
ENSP00000456336.1:n.84-10781T>G
|
|
ENST00000563917.2:n.509T>G
|
|
|
ENST00000565471.6:c.208T>G
|
ENSP00000457384.1:p.Tyr70Asp
|
|
ENST00000635747.1:c.*570T>G
|
ENSP00000490627.1:n.*570T>G
|
|
ENST00000636212.1:c.*337T>G
|
ENSP00000489851.1:n.*337T>G
|
|
ENST00000636674.1:n.1769T>G
|
|
|
ENST00000636964.1:n.2195T>G
|
|
|
ENST00000637054.1:c.198+10127T>G
|
ENSP00000490807.1:n.198+10127T>G
|
|
ENST00000637329.1:c.636T>G
|
|
|
ENST00000637450.1:c.*321T>G
|
ENSP00000490204.1:n.*321T>G
|
|
ENST00000637494.1:c.379T>G
|
ENSP00000490057.1:p.Tyr127Asp
|
|
ENST00000637667.1:c.568T>G
|
ENSP00000489843.1:p.Tyr190Asp
|
|
ENST00000637823.1:c.492T>G
|
|
|
ENST00000637888.1:c.198+10127T>G
|
ENSP00000490546.1:n.198+10127T>G
|
|
ENST00000638076.1:c.*270T>G
|
ENSP00000490373.1:n.*270T>G
|
|
ENST00000638144.1:n.310T>G
|
|
|
ENST00000646164.1:c.39-8728T>G
|
|
|
ENST00000249806.9:c.667T>G
|
ENSP00000249806.5:p.Tyr223Asp
|
|
ENST00000538696.5:c.763T>G
|
ENSP00000445770.1:p.Tyr255Asp
|
|
ENST00000562767.1:c.84-10781T>G
|
ENSP00000456336.1:n.84-10781T>G
|
|
ENST00000564752.1:c.*51T>G
|
ENSP00000457822.1:n.*51T>G
|
|
ENST00000565471.5:c.208T>G
|
ENSP00000457384.1:p.Tyr70Asp
|
|
ENST00000566347.5:c.478T>G
|
ENSP00000457783.1:p.Tyr160Asp
|
|
ENST00000567060.5:c.*65T>G
|
ENSP00000454818.1:n.*65T>G
|
|
NM_017882.2:c.667T>G
|
NP_060352.1:p.Tyr223Asp
|
|
XR_931861.1:n.889T>G
|
|
|
NM_017882.3:c.667T>G
MANE Select
|
NP_060352.1:p.Tyr223Asp
|
|