ENST00000546609.2:n.691T>A
|
|
|
ENST00000713544.1:c.860T>A
|
ENSP00000518840.1:p.Met287Lys
|
|
ENST00000713545.1:c.837T>A
|
ENSP00000518841.1:p.Asp279Glu
|
|
ENST00000228606.9:c.779T>A
MANE Select
|
ENSP00000228606.4:p.Met260Lys
|
|
ENST00000228606.8:c.779T>A
|
ENSP00000228606.4:p.Met260Lys
|
|
ENST00000546567.5:c.74T>A
|
ENSP00000449472.1:p.Met25Lys
|
|
ENST00000546609.1:c.691T>A
|
|
|
ENST00000547344.5:n.918T>A
|
|
|
ENST00000547451.1:n.579T>A
|
|
|
NM_000785.3:c.779T>A
|
NP_000776.1:p.Met260Lys
|
|
NM_000785.4:c.779T>A
MANE Select
|
NP_000776.1:p.Met260Lys
|
|