ENST00000372325.7:c.371-139A>G
MANE Select
|
ENSP00000361400.2:n.371-139A>G
|
|
ENST00000372325.6:c.371-139A>G
|
ENSP00000361400.2:n.371-139A>G
|
|
ENST00000372327.9:c.371-139A>G
|
ENSP00000361402.5:n.371-139A>G
|
|
ENST00000417041.1:c.371-139A>G
|
ENSP00000397375.1:n.371-139A>G
|
|
NM_001098668.2:c.371-139A>G
|
NP_001092138.1:n.371-139A>G
|
|
XM_005270128.2:c.422-139A>G
|
XP_005270185.1:n.422-139A>G
|
|
XM_005270131.3:c.371-139A>G
|
XP_005270188.1:n.371-139A>G
|
|
XM_005270132.3:c.371-139A>G
|
XP_005270189.1:n.371-139A>G
|
|
XM_011540124.1:c.371-139A>G
|
XP_011538426.1:n.371-139A>G
|
|
XM_011540125.1:c.371-139A>G
|
XP_011538427.1:n.371-139A>G
|
|
NM_001098668.3:c.371-139A>G
|
NP_001092138.1:n.371-139A>G
|
|
NM_001320813.1:c.371-139A>G
|
NP_001307742.1:n.371-139A>G
|
|
NM_001320814.1:c.401-139A>G
|
NP_001307743.1:n.401-139A>G
|
|
XM_005270128.3:c.422-139A>G
|
XP_005270185.1:n.422-139A>G
|
|
XM_017016608.1:c.371-139A>G
|
XP_016872097.1:n.371-139A>G
|
|
NM_001098668.4:c.371-139A>G
MANE Select
|
NP_001092138.1:n.371-139A>G
|
|
NM_001320813.2:c.371-139A>G
|
NP_001307742.1:n.371-139A>G
|
|