ENST00000380003.8:c.665+534A>G
MANE Select
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ENSP00000369339.3:n.665+534A>G
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|
ENST00000619707.5:c.665+534A>G
|
ENSP00000482753.1:n.665+534A>G
|
|
ENST00000644136.1:c.665+534A>G
|
ENSP00000494872.1:n.665+534A>G
|
|
ENST00000647196.1:c.665+534A>G
|
ENSP00000494839.1:n.665+534A>G
|
|
ENST00000673600.1:c.665+534A>G
|
ENSP00000500650.1:n.665+534A>G
|
|
ENST00000379997.7:c.*530A>G
|
ENSP00000369333.3:n.*530A>G
|
|
ENST00000380003.7:c.665+534A>G
|
ENSP00000369339.3:n.665+534A>G
|
|
ENST00000488117.5:n.727+534A>G
|
|
|
ENST00000619707.4:c.665+534A>G
|
ENSP00000482753.1:n.665+534A>G
|
|
NM_001256054.2:c.665+534A>G
|
NP_001242983.1:n.665+534A>G
|
|
NM_018325.4:c.665+534A>G
|
NP_060795.1:n.665+534A>G
|
|
NM_145005.6:c.*530A>G
|
NP_659442.2:n.*530A>G
|
|
NM_018325.5:c.665+534A>G
MANE Select
|
NP_060795.1:n.665+534A>G
|
|
NM_001256054.3:c.665+534A>G
|
NP_001242983.1:n.665+534A>G
|
|
NM_145005.7:c.*530A>G
|
NP_659442.2:n.*530A>G
|
|