ENST00000308742.9:c.172-9A>G
MANE Select
|
ENSP00000310120.4:n.172-9A>G
|
|
ENST00000308742.8:c.172-9A>G
|
ENSP00000310120.4:n.172-9A>G
|
|
ENST00000548240.1:c.146-9A>G
|
ENSP00000449210.1:n.146-9A>G
|
|
ENST00000551464.1:c.172-9A>G
|
ENSP00000448819.1:n.172-9A>G
|
|
ENST00000553138.1:n.1486A>G
|
|
|
NM_001013620.3:c.172-9A>G
|
NP_001013642.1:n.172-9A>G
|
|
NM_001308340.1:c.172-9A>G
|
NP_001295269.1:n.172-9A>G
|
|
XM_005268665.3:c.-9-9A>G
|
XP_005268722.1:n.-9-9A>G
|
|
XM_006719243.2:c.-9-9A>G
|
XP_006719306.1:n.-9-9A>G
|
|
XM_005268665.4:c.-9-9A>G
|
XP_005268722.1:n.-9-9A>G
|
|
NM_001013620.4:c.172-9A>G
MANE Select
|
NP_001013642.2:n.172-9A>G
|
|
NM_001308340.2:c.172-9A>G
|
NP_001295269.2:n.172-9A>G
|
|