ENST00000546609.2:n.299-169G>A
|
|
|
ENST00000713544.1:c.387-88G>A
|
ENSP00000518840.1:n.387-88G>A
|
|
ENST00000713545.1:c.387-111G>A
|
ENSP00000518841.1:n.387-111G>A
|
|
ENST00000228606.9:c.387-169G>A
MANE Select
|
ENSP00000228606.4:n.387-169G>A
|
|
ENST00000228606.8:c.387-169G>A
|
ENSP00000228606.4:n.387-169G>A
|
|
ENST00000546496.1:n.215-169G>A
|
|
|
ENST00000546567.5:c.-488G>A
|
ENSP00000449472.1:n.-488G>A
|
|
ENST00000546609.1:c.299-169G>A
|
|
|
ENST00000547344.5:n.441-169G>A
|
|
|
ENST00000547451.1:n.18G>A
|
|
|
ENST00000552186.1:n.506-169G>A
|
|
|
NM_000785.3:c.387-169G>A
|
NP_000776.1:n.387-169G>A
|
|
NM_000785.4:c.387-169G>A
MANE Select
|
NP_000776.1:n.387-169G>A
|
|