ENST00000546609.2:n.299-195G=
|
|
|
ENST00000713544.1:c.387-114G=
|
ENSP00000518840.1:n.387-114G=
|
|
ENST00000713545.1:c.387-137G=
|
ENSP00000518841.1:n.387-137G=
|
|
ENST00000228606.9:c.387-195G=
MANE Select
|
ENSP00000228606.4:n.387-195G=
|
|
ENST00000228606.8:c.387-195G=
|
ENSP00000228606.4:n.387-195G=
|
|
ENST00000546496.1:n.215-195G=
|
|
|
ENST00000546609.1:c.299-195G=
|
|
|
ENST00000547344.5:n.441-195G=
|
|
|
ENST00000552186.1:n.506-195G=
|
|
|
NM_000785.3:c.387-195G=
|
NP_000776.1:n.387-195G=
|
|
NM_000785.4:c.387-195G=
MANE Select
|
NP_000776.1:n.387-195G=
|
|