ENST00000674537.2:c.1452+92C>G
|
ENSP00000502725.1:n.1452+92C>G
|
|
ENST00000392302.7:c.1452+92C>G
|
ENSP00000376120.3:n.1452+92C>G
|
|
ENST00000497019.7:c.*224+92C>G
|
ENSP00000436804.2:n.*224+92C>G
|
|
ENST00000524377.7:c.1632+92C>G
MANE Select
|
ENSP00000431418.1:n.1632+92C>G
|
|
ENST00000674537.1:c.1452+92C>G
|
ENSP00000502725.1:n.1452+92C>G
|
|
ENST00000358660.3:c.1623+92C>G
|
ENSP00000351486.3:n.1623+92C>G
|
|
ENST00000368196.7:c.1614+92C>G
|
ENSP00000357179.3:n.1614+92C>G
|
|
ENST00000392302.6:c.1524+92C>G
|
ENSP00000376120.2:n.1524+92C>G
|
|
ENST00000497019.6:c.*224+92C>G
|
ENSP00000436804.1:n.*224+92C>G
|
|
ENST00000524377.5:c.1632+92C>G
|
ENSP00000431418.1:n.1632+92C>G
|
|
ENST00000530298.5:n.2085+92C>G
|
|
|
NM_001007792.1:c.1524+92C>G , LRG_261t1:c.1524+92C>G
|
NP_001007793.1:n.1524+92C>G
|
|
NM_001012331.1:c.1614+92C>G , LRG_261t2:c.1614+92C>G
|
NP_001012331.1:n.1614+92C>G
|
|
NM_002529.3:c.1632+92C>G , LRG_261t3:c.1632+92C>G
|
NP_002520.2:n.1632+92C>G
|
|
NM_001012331.2:c.1614+92C>G
|
NP_001012331.1:n.1614+92C>G
|
|
NM_002529.4:c.1632+92C>G
MANE Select
|
NP_002520.2:n.1632+92C>G
|
|