ENST00000297494.8:c.1647+33A>G
MANE Select
|
ENSP00000297494.3:n.1647+33A>G
|
|
ENST00000297494.7:c.1647+33A>G
|
ENSP00000297494.3:n.1647+33A>G
|
|
ENST00000460603.1:n.99+33A>G
|
|
|
ENST00000461406.5:c.1029+33A>G
|
ENSP00000417143.1:n.1029+33A>G
|
|
ENST00000467517.1:c.1647+33A>G
|
ENSP00000420551.1:n.1647+33A>G
|
|
ENST00000484524.5:c.1647+33A>G
|
ENSP00000420215.1:n.1647+33A>G
|
|
NM_000603.4:c.1647+33A>G
|
NP_000594.2:n.1647+33A>G
|
|
NM_001160109.1:c.1647+33A>G
|
NP_001153581.1:n.1647+33A>G
|
|
NM_001160110.1:c.1647+33A>G
|
NP_001153582.1:n.1647+33A>G
|
|
NM_001160111.1:c.1647+33A>G
|
NP_001153583.1:n.1647+33A>G
|
|
XM_006716002.2:c.1647+33A>G
|
XP_006716065.1:n.1647+33A>G
|
|
NM_000603.5:c.1647+33A>G
MANE Select
|
NP_000594.2:n.1647+33A>G
|
|
NM_001160109.2:c.1647+33A>G
|
NP_001153581.1:n.1647+33A>G
|
|