ENST00000615234.5:c.429+104T>G
MANE Select
|
ENSP00000478303.1:n.429+104T>G
|
|
ENST00000215587.11:c.429+104T>G
|
ENSP00000215587.7:n.429+104T>G
|
|
ENST00000585838.2:c.200+104T>G
|
|
|
ENST00000586746.5:c.429+104T>G
|
ENSP00000464739.1:n.429+104T>G
|
|
ENST00000586817.5:n.1669+104T>G
|
|
|
ENST00000589737.5:c.*98+104T>G
|
ENSP00000467905.1:n.*98+104T>G
|
|
ENST00000590060.5:c.231+104T>G
|
ENSP00000479560.1:n.231+104T>G
|
|
ENST00000591767.5:c.*195+104T>G
|
ENSP00000465066.1:n.*195+104T>G
|
|
ENST00000612655.4:c.429+104T>G
|
ENSP00000485021.1:n.429+104T>G
|
|
ENST00000614705.4:n.468+104T>G
|
|
|
ENST00000615234.4:c.429+104T>G
|
ENSP00000478303.1:n.429+104T>G
|
|
ENST00000619917.4:c.349-659T>G
|
ENSP00000479813.1:n.349-659T>G
|
|
NM_001316323.1:c.150+104T>G
|
NP_001303252.1:n.150+104T>G
|
|
NM_001316324.1:c.150+104T>G
|
NP_001303253.1:n.150+104T>G
|
|
NM_002695.3:c.429+104T>G
|
NP_002686.2:n.429+104T>G
|
|
XM_011528070.1:c.429+104T>G
|
XP_011526372.1:n.429+104T>G
|
|
XM_011528070.3:c.429+104T>G
|
XP_011526372.1:n.429+104T>G
|
|
XM_017026883.2:c.150+104T>G
|
XP_016882372.1:n.150+104T>G
|
|
NM_002695.4:c.429+104T>G
|
NP_002686.2:n.429+104T>G
|
|
NM_001316323.2:c.150+104T>G
|
NP_001303252.1:n.150+104T>G
|
|
NM_001316324.2:c.150+104T>G
|
NP_001303253.1:n.150+104T>G
|
|
NM_002695.5:c.429+104T>G
MANE Select
|
NP_002686.3:n.429+104T>G
|
|