|
ENST00000463956.2:n.431+66G>T
|
|
|
|
ENST00000484513.2:n.2000G>T
|
|
|
|
ENST00000699084.1:n.1611G>T
|
|
|
|
ENST00000699085.1:n.1509+66G>T
|
|
|
|
ENST00000699086.1:c.425+85G>T
|
|
|
|
ENST00000396334.8:c.644+66G>T
|
ENSP00000379625.4:n.644+66G>T
|
|
|
ENST00000416282.3:n.625G>T
|
|
|
|
ENST00000417037.8:c.509+66G>T
|
ENSP00000401399.4:n.509+66G>T
|
|
|
ENST00000421516.3:c.668+42G>T
|
ENSP00000391753.3:n.668+42G>T
|
|
|
ENST00000650112.2:c.329-123G>T
|
ENSP00000497991.2:n.329-123G>T
|
|
|
ENST00000650905.2:c.644+66G>T
MANE Select
|
ENSP00000498360.2:n.644+66G>T
|
|
|
ENST00000651800.2:c.464-123G>T
|
ENSP00000499012.2:n.464-123G>T
|
|
|
ENST00000652213.1:c.625+85G>T
|
ENSP00000498576.1:n.625+85G>T
|
|
|
ENST00000652590.1:n.750G>T
|
|
|
|
ENST00000396334.7:c.683+66G>T
|
ENSP00000379625.3:n.683+66G>T
|
|
|
ENST00000416282.2:n.625G>T
|
|
|
|
ENST00000417037.6:c.707+42G>T
|
ENSP00000401399.2:n.707+42G>T
|
|
|
ENST00000421516.1:c.704+42G>T
|
ENSP00000391753.1:n.704+42G>T
|
|
|
ENST00000424893.5:c.548+66G>T
|
ENSP00000389979.1:n.548+66G>T
|
|
|
ENST00000443433.6:c.503-123G>T
|
ENSP00000390565.2:n.503-123G>T
|
|
|
ENST00000463956.1:n.357+66G>T
|
|
|
|
ENST00000481122.5:n.437+66G>T
|
|
|
|
ENST00000484513.1:n.1212G>T
|
|
|
|
ENST00000495303.5:c.368-123G>T
|
ENSP00000417848.1:n.368-123G>T
|
|
|
NM_001172566.1:c.368-123G>T
|
NP_001166037.1:n.368-123G>T
|
|
|
NM_001172567.1:c.707+42G>T , LRG_157t1:c.707+42G>T
|
NP_001166038.1:n.707+42G>T
|
|
|
NM_001172568.1:c.548+66G>T
|
NP_001166039.1:n.548+66G>T
|
|
|
NM_001172569.1:c.503-123G>T
|
NP_001166040.1:n.503-123G>T
|
|
|
NM_002468.4:c.683+66G>T
|
NP_002459.2:n.683+66G>T
|
|
|
XM_005265172.1:c.664+85G>T
|
XP_005265229.1:n.664+85G>T
|
|
|
XM_006713170.1:c.529+85G>T
|
XP_006713233.1:n.529+85G>T
|
|
|
NM_001172566.2:c.329-123G>T
|
NP_001166037.2:n.329-123G>T
|
|
|
NM_001172567.2:c.668+42G>T
|
NP_001166038.2:n.668+42G>T
|
|
|
NM_001172568.2:c.509+66G>T
|
NP_001166039.2:n.509+66G>T
|
|
|
NM_001172569.2:c.464-123G>T
|
NP_001166040.2:n.464-123G>T
|
|
|
NM_001365876.1:c.625+85G>T
|
NP_001352805.1:n.625+85G>T
|
|
|
NM_001365877.1:c.490+85G>T
|
NP_001352806.1:n.490+85G>T
|
|
|
NM_002468.5:c.644+66G>T
MANE Select
|
NP_002459.3:n.644+66G>T
|
|
|
NM_001172569.3:c.464-123G>T
|
NP_001166040.2:n.464-123G>T
|
|
|
NM_001374787.1:c.644+66G>T
|
NP_001361716.1:n.644+66G>T
|
|
|
NM_001374788.1:c.176+66G>T
|
NP_001361717.1:n.176+66G>T
|
|
|
NR_164663.1:n.327+85G>T
|
|
|
