ENST00000446859.7:c.908+4A>T
MANE Select
|
ENSP00000414635.1:n.908+4A>T
|
|
ENST00000446859.5:c.908+4A>T
|
ENSP00000414635.1:n.908+4A>T
|
|
ENST00000522080.5:n.885+4A>T
|
|
|
ENST00000522329.1:n.157+4A>T
|
|
|
ENST00000522526.6:c.812+4A>T
|
ENSP00000429278.2:n.812+4A>T
|
|
ENST00000522596.6:n.890+4A>T
|
|
|
ENST00000522830.5:c.725+4A>T
|
ENSP00000429593.1:n.725+4A>T
|
|
ENST00000524327.5:n.708+4A>T
|
|
|
ENST00000528597.1:c.155+4A>T
|
ENSP00000436883.1:n.155+4A>T
|
|
ENST00000602774.1:n.298A>T
|
|
|
NM_001172779.1:c.908+4A>T
|
NP_001166250.1:n.908+4A>T
|
|
NM_001172780.1:c.908+4A>T
|
NP_001166251.1:n.908+4A>T
|
|
NM_153353.4:c.812+4A>T
|
NP_699184.2:n.812+4A>T
|
|
XM_005247133.2:c.725+4A>T
|
XP_005247190.1:n.725+4A>T
|
|
XM_006713508.2:c.854+4A>T
|
XP_006713571.1:n.854+4A>T
|
|
XM_011512442.1:c.905+4A>T
|
XP_011510744.1:n.905+4A>T
|
|
NM_001363888.1:c.725+4A>T
|
NP_001350817.1:n.725+4A>T
|
|
XM_006713508.4:c.854+4A>T
|
XP_006713571.1:n.854+4A>T
|
|
XM_011512442.2:c.905+4A>T
|
XP_011510744.1:n.905+4A>T
|
|
XM_017005746.1:c.722+4A>T
|
XP_016861235.1:n.722+4A>T
|
|
NM_001172779.2:c.908+4A>T
MANE Select
|
NP_001166250.1:n.908+4A>T
|
|
NM_001172780.2:c.908+4A>T
|
NP_001166251.1:n.908+4A>T
|
|
NM_001363888.2:c.725+4A>T
|
NP_001350817.1:n.725+4A>T
|
|
NM_001370608.1:c.722+4A>T
|
NP_001357537.1:n.722+4A>T
|
|
NM_001370609.1:c.725+4A>T
|
NP_001357538.1:n.725+4A>T
|
|
NM_153353.5:c.812+4A>T
|
NP_699184.2:n.812+4A>T
|
|