ENST00000546609.2:n.298+221G>T
|
|
|
ENST00000713544.1:c.387-206G>T
|
ENSP00000518840.1:n.387-206G>T
|
|
ENST00000713545.1:c.386+221G>T
|
ENSP00000518841.1:n.386+221G>T
|
|
ENST00000228606.9:c.386+221G>T
MANE Select
|
ENSP00000228606.4:n.386+221G>T
|
|
ENST00000228606.8:c.386+221G>T
|
ENSP00000228606.4:n.386+221G>T
|
|
ENST00000546496.1:n.214+221G>T
|
|
|
ENST00000546609.1:c.298+221G>T
|
|
|
ENST00000547344.5:n.440+221G>T
|
|
|
ENST00000552186.1:n.505+221G>T
|
|
|
NM_000785.3:c.386+221G>T
|
NP_000776.1:n.386+221G>T
|
|
NM_000785.4:c.386+221G>T
MANE Select
|
NP_000776.1:n.386+221G>T
|
|