ENST00000585362.7:c.588-185_588-184insCTGCA
|
ENSP00000473614.3:n.588-185_588-184insCTGCA
|
|
ENST00000593032.6:c.396-124_396-123insCTGCA
|
ENSP00000465828.4:n.396-124_396-123insCTGCA
|
|
ENST00000706713.1:c.471-185_471-184insCTGCA
|
ENSP00000516510.1:n.471-185_471-184insCTGCA
|
|
ENST00000706714.1:c.396-124_396-123insCTGCA
|
ENSP00000516511.1:n.396-124_396-123insCTGCA
|
|
ENST00000706715.1:c.93-185_93-184insCTGCA
|
ENSP00000516512.1:n.93-185_93-184insCTGCA
|
|
ENST00000354171.13:c.477-185_477-184insCTGCA
MANE Select
|
ENSP00000346103.7:n.477-185_477-184insCTGCA
|
|
ENST00000589115.6:c.476+248_476+249insCTGCA
|
ENSP00000466872.3:n.476+248_476+249insCTGCA
|
|
ENST00000354171.12:c.477-185_477-184insCTGCA
|
ENSP00000346103.7:n.477-185_477-184insCTGCA
|
|
ENST00000585480.1:c.210-185_210-184insCTGCA
|
ENSP00000467900.1:n.210-185_210-184insCTGCA
|
|
ENST00000587648.5:c.357-185_357-184insCTGCA
|
ENSP00000468349.1:n.357-185_357-184insCTGCA
|
|
ENST00000588919.5:c.396-185_396-184insCTGCA
|
ENSP00000464989.3:n.396-185_396-184insCTGCA
|
|
ENST00000589115.5:c.476+248_476+249insCTGCA
|
ENSP00000466872.2:n.476+248_476+249insCTGCA
|
|
ENST00000592940.2:n.663_664insCTGCA
|
|
|
ENST00000593032.5:c.396-124_396-123insCTGCA
|
ENSP00000465828.3:n.396-124_396-123insCTGCA
|
|
ENST00000611653.4:c.396-185_396-184insCTGCA
|
ENSP00000483655.1:n.396-185_396-184insCTGCA
|
|
ENST00000616066.4:c.474-185_474-184insCTGCA
|
ENSP00000485000.1:n.474-185_474-184insCTGCA
|
|
ENST00000622390.4:c.585-185_585-184insCTGCA
|
ENSP00000477503.1:n.585-185_585-184insCTGCA
|
|
NM_001039847.2:c.477-185_477-184insCTGCA
|
NP_001034936.1:n.477-185_477-184insCTGCA
|
|
NM_001039848.2:c.588-185_588-184insCTGCA
|
NP_001034937.1:n.588-185_588-184insCTGCA
|
|
NM_002085.4:c.477-185_477-184insCTGCA
|
NP_002076.2:n.477-185_477-184insCTGCA
|
|
NM_001039848.3:c.588-185_588-184insCTGCA
|
NP_001034937.1:n.588-185_588-184insCTGCA
|
|
NM_001039847.3:c.477-185_477-184insCTGCA
|
NP_001034936.1:n.477-185_477-184insCTGCA
|
|
NM_001039848.4:c.588-185_588-184insCTGCA
|
NP_001034937.1:n.588-185_588-184insCTGCA
|
|
NM_001367832.1:c.396-185_396-184insCTGCA
|
NP_001354761.1:n.396-185_396-184insCTGCA
|
|
NM_002085.5:c.477-185_477-184insCTGCA
MANE Select
|
NP_002076.2:n.477-185_477-184insCTGCA
|
|