ENST00000643606.3:c.211+362C>A
MANE Select
|
ENSP00000494576.2:n.211+362C>A
|
|
ENST00000644830.1:c.52+362C>A
|
ENSP00000495111.1:n.52+362C>A
|
|
ENST00000651652.1:c.109+362C>A
|
ENSP00000498953.1:n.109+362C>A
|
|
ENST00000326431.3:c.211+362C>A
|
ENSP00000324775.3:n.211+362C>A
|
|
NM_147196.2:c.211+362C>A
|
NP_671729.2:n.211+362C>A
|
|
XM_006713097.2:c.52+362C>A
|
XP_006713160.1:n.52+362C>A
|
|
XM_011533574.1:c.52+362C>A
|
XP_011531876.1:n.52+362C>A
|
|
XM_006713097.4:c.52+362C>A
|
XP_006713160.1:n.52+362C>A
|
|
XM_024453446.1:c.52+362C>A
|
XP_024309214.1:n.52+362C>A
|
|
NM_001370524.1:c.52+362C>A
|
NP_001357453.1:n.52+362C>A
|
|
NM_001370525.1:c.52+362C>A
|
NP_001357454.1:n.52+362C>A
|
|
NM_147196.3:c.211+362C>A
MANE Select
|
NP_671729.2:n.211+362C>A
|
|