ENST00000336098.8:c.*155_*156insT
MANE Select
|
ENSP00000336829.3:n.*155_*156insT
|
|
ENST00000336098.7:c.*155_*156insT
|
ENSP00000336829.3:n.*155_*156insT
|
|
ENST00000404648.7:c.1299+218_1299+219insT
|
ENSP00000384860.3:n.1299+218_1299+219insT
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|
ENST00000405164.5:c.1323+218_1323+219insT
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ENSP00000384101.1:n.1323+218_1323+219insT
|
|
ENST00000407946.5:c.*155_*156insT
|
ENSP00000384552.1:n.*155_*156insT
|
|
ENST00000465913.1:n.1065_1066insT
|
|
|
ENST00000492082.5:n.1841+218_1841+219insT
|
|
|
NM_000509.4:c.1299+218_1299+219insT
|
NP_000500.2:n.1299+218_1299+219insT
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|
NM_000509.5:c.1299+218_1299+219insT
|
NP_000500.2:n.1299+218_1299+219insT
|
|
NM_021870.2:c.*155_*156insT
|
NP_068656.2:n.*155_*156insT
|
|
NM_021870.3:c.*155_*156insT
MANE Select
|
NP_068656.2:n.*155_*156insT
|
|
NM_000509.6:c.1299+218_1299+219insT
|
NP_000500.2:n.1299+218_1299+219insT
|
|