ENST00000301761.7:c.*11A>T
MANE Select
|
ENSP00000301761.3:n.*11A>T
|
|
ENST00000301761.6:c.*11A>T
|
ENSP00000301761.2:n.*11A>T
|
|
ENST00000536670.5:n.396+7969A>T
|
|
|
ENST00000538594.5:c.370+7969A>T
|
ENSP00000440939.1:n.370+7969A>T
|
|
ENST00000541135.5:c.377+7962A>T
|
ENSP00000443130.1:n.377+7962A>T
|
|
ENST00000542074.1:c.*91A>T
|
ENSP00000469670.1:n.*91A>T
|
|
ENST00000542794.5:c.*514A>T
|
ENSP00000439983.1:n.*514A>T
|
|
ENST00000543044.2:c.*11A>T
|
ENSP00000440219.1:n.*11A>T
|
|
ENST00000543265.1:c.*135A>T
|
ENSP00000443660.1:n.*135A>T
|
|
ENST00000544025.5:n.465+7969A>T
|
|
|
ENST00000544801.5:c.370+7969A>T
|
ENSP00000442581.1:n.370+7969A>T
|
|
ENST00000544880.1:n.374+7969A>T
|
|
|
NM_017841.2:c.*11A>T , LRG_519t1:c.*11A>T
|
NP_060311.1:n.*11A>T
|
|
NM_017841.4:c.*11A>T
MANE Select
|
NP_060311.1:n.*11A>T
|
|