ENST00000334660.10:c.411+1106T>A
MANE Select
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ENSP00000335632.5:n.411+1106T>A
|
|
ENST00000334660.9:c.411+1106T>A
|
ENSP00000335632.5:n.411+1106T>A
|
|
ENST00000392151.6:c.350-7043T>A
|
ENSP00000440490.1:n.350-7043T>A
|
|
ENST00000558351.5:n.543+1106T>A
|
|
|
ENST00000560397.5:c.411+1106T>A
|
ENSP00000454007.1:n.411+1106T>A
|
|
ENST00000560411.5:c.*176+1106T>A
|
ENSP00000453375.1:n.*176+1106T>A
|
|
ENST00000560633.1:n.399-456T>A
|
|
|
ENST00000560784.5:c.*110+1106T>A
|
ENSP00000452772.1:n.*110+1106T>A
|
|
ENST00000560965.1:c.272-456T>A
|
|
|
NM_007236.4:c.411+1106T>A
|
NP_009167.1:n.411+1106T>A
|
|
NM_007236.5:c.411+1106T>A
MANE Select
|
NP_009167.1:n.411+1106T>A
|
|