ENST00000450046.2:c.2787+291A>T
|
ENSP00000413354.2:n.2787+291A>T
|
|
ENST00000700145.1:c.900-4643A>T
|
|
|
ENST00000700146.1:n.690+291A>T
|
|
|
ENST00000700147.1:n.132A>T
|
|
|
ENST00000275493.7:c.2946+291A>T
MANE Select
|
ENSP00000275493.2:n.2946+291A>T
|
|
ENST00000275493.6:c.2946+291A>T
|
ENSP00000275493.2:n.2946+291A>T
|
|
ENST00000442591.5:c.*28+27776A>T
|
ENSP00000410031.1:n.*28+27776A>T
|
|
ENST00000454757.6:c.2811+291A>T
|
ENSP00000395243.3:n.2811+291A>T
|
|
ENST00000455089.5:c.2811+291A>T
|
ENSP00000415559.1:n.2811+291A>T
|
|
ENST00000485503.1:n.567A>T
|
|
|
NM_005228.3:c.2946+291A>T , LRG_304t1:c.2946+291A>T
|
NP_005219.2:n.2946+291A>T
|
|
NM_001346897.1:c.2811+291A>T
|
NP_001333826.1:n.2811+291A>T
|
|
NM_001346898.1:c.2946+291A>T
|
NP_001333827.1:n.2946+291A>T
|
|
NM_001346899.1:c.2811+291A>T
|
NP_001333828.1:n.2811+291A>T
|
|
NM_001346900.1:c.2787+291A>T
|
NP_001333829.1:n.2787+291A>T
|
|
NM_001346941.1:c.2145+291A>T
|
NP_001333870.1:n.2145+291A>T
|
|
NM_005228.4:c.2946+291A>T
|
NP_005219.2:n.2946+291A>T
|
|
NM_005228.5:c.2946+291A>T
MANE Select
|
NP_005219.2:n.2946+291A>T
|
|
NM_001346897.2:c.2811+291A>T
|
NP_001333826.1:n.2811+291A>T
|
|
NM_001346898.2:c.2946+291A>T
|
NP_001333827.1:n.2946+291A>T
|
|
NM_001346900.2:c.2787+291A>T
|
NP_001333829.1:n.2787+291A>T
|
|
NM_001346941.2:c.2145+291A>T
|
NP_001333870.1:n.2145+291A>T
|
|
NM_001346899.2:c.2811+291A>T
|
NP_001333828.1:n.2811+291A>T
|
|