ENST00000546609.2:n.574T>A
|
|
|
ENST00000713544.1:c.743T>A
|
ENSP00000518840.1:p.Phe248Tyr
|
|
ENST00000713545.1:c.720T>A
|
ENSP00000518841.1:p.Leu240=
|
|
ENST00000228606.9:c.662T>A
MANE Select
|
ENSP00000228606.4:p.Phe221Tyr
|
|
ENST00000228606.8:c.662T>A
|
ENSP00000228606.4:p.Phe221Tyr
|
|
ENST00000546567.5:c.-44T>A
|
ENSP00000449472.1:n.-44T>A
|
|
ENST00000546609.1:c.574T>A
|
|
|
ENST00000547344.5:n.801T>A
|
|
|
ENST00000547451.1:n.462T>A
|
|
|
NM_000785.3:c.662T>A
|
NP_000776.1:p.Phe221Tyr
|
|
NM_000785.4:c.662T>A
MANE Select
|
NP_000776.1:p.Phe221Tyr
|
|