ENST00000418931.7:c.364+1567A>C
MANE Select
|
ENSP00000408146.2:n.364+1567A>C
|
|
ENST00000416804.1:c.264+1567A>C
|
|
|
ENST00000418931.6:c.364+1567A>C
|
ENSP00000408146.2:n.364+1567A>C
|
|
ENST00000428835.5:c.295+1567A>C
|
ENSP00000412654.1:n.295+1567A>C
|
|
ENST00000471184.5:n.414-1012A>C
|
|
|
ENST00000478189.1:n.423+364A>C
|
|
|
ENST00000488575.1:n.413+1567A>C
|
|
|
ENST00000498038.1:n.493+1567A>C
|
|
|
NM_002121.5:c.364+1567A>C
|
NP_002112.3:n.364+1567A>C
|
|
XM_006715078.2:c.52+1567A>C
|
XP_006715141.1:n.52+1567A>C
|
|
NM_002121.6:c.364+1567A>C
MANE Select
|
NP_002112.3:n.364+1567A>C
|
|