ENST00000636937.2:c.2246T>A
|
ENSP00000516154.1:p.Phe749Tyr
|
|
ENST00000268124.11:c.2246T>A
MANE Select
|
ENSP00000268124.5:p.Phe749Tyr
|
|
ENST00000530292.3:c.1847T>A
|
ENSP00000432885.2:p.Phe616Tyr
|
|
ENST00000635986.2:c.2246T>A
|
ENSP00000490653.2:p.Phe749Tyr
|
|
ENST00000636774.1:c.*813T>A
|
ENSP00000489799.1:n.*813T>A
|
|
ENST00000637238.1:c.943T>A
|
ENSP00000490756.1:n.943T>A
|
|
ENST00000637264.1:c.1318T>A
|
|
|
ENST00000666746.1:c.1823T>A
|
|
|
ENST00000670281.1:c.566T>A
|
ENSP00000499709.1:p.Phe189Tyr
|
|
ENST00000672071.1:n.2444T>A
|
|
|
ENST00000672923.2:n.2349T>A
|
|
|
ENST00000268124.9:c.2246T>A
|
ENSP00000268124.5:p.Phe749Tyr
|
|
ENST00000442287.6:c.2246T>A
|
ENSP00000399851.2:p.Phe749Tyr
|
|
ENST00000526314.2:c.539+392T>A
|
|
|
ENST00000526398.1:c.395T>A
|
|
|
ENST00000528881.2:c.15T>A
|
|
|
ENST00000530715.5:c.5T>A
|
ENSP00000431395.1:p.Phe2Tyr
|
|
ENST00000532584.5:n.448T>A
|
|
|
ENST00000631044.2:c.*1670T>A
|
ENSP00000486730.1:n.*1670T>A
|
|
NM_001126131.1:c.2246T>A
|
NP_001119603.1:p.Phe749Tyr
|
|
NM_002693.2:c.2246T>A
|
NP_002684.1:p.Phe749Tyr
|
|
NM_001126131.2:c.2246T>A
|
NP_001119603.1:p.Phe749Tyr
|
|
NM_002693.3:c.2246T>A
MANE Select
|
NP_002684.1:p.Phe749Tyr
|
|