|
NM_007202.4:c.1323-4A>G
MANE Select
|
NP_009133.2:n.1323-4A>G
|
|
ENST00000225737.11:c.1323-4A>G
MANE Select
|
ENSP00000225737.6:n.1323-4A>G
|
|
NM_001330152.1:c.1323-4A>G
|
NP_001317081.1:n.1323-4A>G
|
|
NM_001330152.2:c.1323-4A>G
|
NP_001317081.1:n.1323-4A>G
|
|
NM_007202.3:c.1323-4A>G
|
NP_009133.2:n.1323-4A>G
|
|
ENST00000225737.10:c.1323-4A>G
|
ENSP00000225737.6:n.1323-4A>G
|
|
ENST00000395536.7:c.1323-4A>G
|
ENSP00000378907.3:n.1323-4A>G
|
|
ENST00000460046.2:c.292-4A>G
|
|
|
XM_006721431.2:c.1323-4A>G
|
XP_006721494.1:n.1323-4A>G
|
|
XM_006721432.2:c.1323-4A>G
|
XP_006721495.1:n.1323-4A>G
|
|
XR_001752417.2:n.1464-4A>G
|
|
|
XR_001752418.2:n.1435-4A>G
|
|
|
XR_243536.1:n.1357-4A>G
|
|
|
XR_243536.3:n.1340-4A>G
|
|
|
XR_933969.1:n.1481-4A>G
|
|
|
XR_933969.3:n.1464-4A>G
|
|
|
XR_933970.1:n.1481-4A>G
|
|