ENST00000698727.1:n.1676+100T>A
|
|
|
ENST00000698728.1:n.2195+100T>A
|
|
|
ENST00000698729.1:n.3741+100T>A
|
|
|
ENST00000698730.1:n.3741+100T>A
|
|
|
ENST00000698731.1:c.2475+100T>A
|
ENSP00000513898.1:n.2475+100T>A
|
|
ENST00000698732.1:c.*1477+100T>A
|
ENSP00000513899.1:n.*1477+100T>A
|
|
ENST00000698733.1:c.*1803+100T>A
|
ENSP00000513900.1:n.*1803+100T>A
|
|
ENST00000698734.1:c.2616+100T>A
|
ENSP00000513901.1:n.2616+100T>A
|
|
ENST00000698735.1:n.2731+100T>A
|
|
|
ENST00000698736.1:n.2731+100T>A
|
|
|
ENST00000698737.1:n.2731+100T>A
|
|
|
ENST00000698738.1:n.2731+100T>A
|
|
|
ENST00000698739.1:n.2731+100T>A
|
|
|
ENST00000372371.8:c.2616+100T>A
MANE Select
|
ENSP00000361446.3:n.2616+100T>A
|
|
ENST00000372371.7:c.2616+100T>A
|
ENSP00000361446.3:n.2616+100T>A
|
|
ENST00000472014.5:n.469+4835T>A
|
|
|
NM_007055.3:c.2616+100T>A
|
NP_008986.2:n.2616+100T>A
|
|
NM_007055.4:c.2616+100T>A
MANE Select
|
NP_008986.2:n.2616+100T>A
|
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