ENST00000643672.1:c.741+12A>G
|
ENSP00000494532.1:n.741+12A>G
|
|
ENST00000645280.1:c.738+12A>G
|
ENSP00000496690.1:n.738+12A>G
|
|
ENST00000648579.1:c.*89+12A>G
|
ENSP00000497638.1:n.*89+12A>G
|
|
ENST00000650617.1:c.792+12A>G
MANE Select
|
ENSP00000497532.1:n.792+12A>G
|
|
ENST00000273158.8:c.792+12A>G
|
ENSP00000273158.3:n.792+12A>G
|
|
NM_017875.2:c.792+12A>G
|
NP_060345.2:n.792+12A>G
|
|
XM_006713214.1:c.780+12A>G
|
XP_006713277.1:n.780+12A>G
|
|
XM_011533869.1:c.774+12A>G
|
XP_011532171.1:n.774+12A>G
|
|
XM_011533870.1:c.741+12A>G
|
XP_011532172.1:n.741+12A>G
|
|
XM_011533871.1:c.612+12A>G
|
XP_011532173.1:n.612+12A>G
|
|
NM_001354798.1:c.626-1810A>G
|
NP_001341727.1:n.626-1810A>G
|
|
NM_017875.4:c.792+12A>G
MANE Select
|
NP_060345.2:n.792+12A>G
|
|
XM_006713214.2:c.780+12A>G
|
XP_006713277.1:n.780+12A>G
|
|
XM_011533869.2:c.774+12A>G
|
XP_011532171.1:n.774+12A>G
|
|
XM_024453611.1:c.738+12A>G
|
XP_024309379.1:n.738+12A>G
|
|
NM_001354798.2:c.626-1810A>G
|
NP_001341727.1:n.626-1810A>G
|
|