ENST00000546609.2:n.298+241A>C
|
|
|
ENST00000713544.1:c.387-186A>C
|
ENSP00000518840.1:n.387-186A>C
|
|
ENST00000713545.1:c.387-209A>C
|
ENSP00000518841.1:n.387-209A>C
|
|
ENST00000228606.9:c.386+241A>C
MANE Select
|
ENSP00000228606.4:n.386+241A>C
|
|
ENST00000228606.8:c.386+241A>C
|
ENSP00000228606.4:n.386+241A>C
|
|
ENST00000546496.1:n.214+241A>C
|
|
|
ENST00000546609.1:c.298+241A>C
|
|
|
ENST00000547344.5:n.440+241A>C
|
|
|
ENST00000552186.1:n.505+241A>C
|
|
|
NM_000785.3:c.386+241A>C
|
NP_000776.1:n.386+241A>C
|
|
NM_000785.4:c.386+241A>C
MANE Select
|
NP_000776.1:n.386+241A>C
|
|