ENST00000424296.7:c.-12+4703T>A
MANE Select
|
ENSP00000410186.2:n.-12+4703T>A
|
|
ENST00000285397.9:c.-12+4703T>A
|
ENSP00000285397.4:n.-12+4703T>A
|
|
ENST00000368948.6:c.-12+4703T>A
|
ENSP00000357944.2:n.-12+4703T>A
|
|
ENST00000424296.6:c.-12+4703T>A
|
ENSP00000410186.2:n.-12+4703T>A
|
|
ENST00000448084.6:c.-115+4028T>A
|
ENSP00000407510.2:n.-115+4028T>A
|
|
ENST00000532976.1:c.-12+4028T>A
|
ENSP00000436325.1:n.-12+4028T>A
|
|
NM_001145128.2:c.-12+4703T>A
|
NP_001138600.2:n.-12+4703T>A
|
|
NM_145025.4:c.-12+4703T>A
|
NP_659462.1:n.-12+4703T>A
|
|
XM_006715376.2:c.-12-384T>A
|
XP_006715439.2:n.-12-384T>A
|
|
XM_011535550.1:c.-12-384T>A
|
XP_011533852.1:n.-12-384T>A
|
|
XM_011535551.1:c.-12-384T>A
|
XP_011533853.1:n.-12-384T>A
|
|
XM_011535552.1:c.-12+4703T>A
|
XP_011533854.1:n.-12+4703T>A
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|
XM_011535553.1:c.-12+4028T>A
|
XP_011533855.1:n.-12+4028T>A
|
|
XM_011535554.1:c.-12-384T>A
|
XP_011533856.1:n.-12-384T>A
|
|
XM_011535555.1:c.-12-384T>A
|
XP_011533857.1:n.-12-384T>A
|
|
XM_011535556.1:c.-12-384T>A
|
XP_011533858.1:n.-12-384T>A
|
|
XM_011535557.1:c.-12-384T>A
|
XP_011533859.1:n.-12-384T>A
|
|
XM_011535559.1:c.-12-384T>A
|
XP_011533861.1:n.-12-384T>A
|
|
XR_942337.1:n.674-384T>A
|
|
|
XR_942338.1:n.674-384T>A
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|
|
NM_001329602.1:c.-12+4028T>A
|
NP_001316531.1:n.-12+4028T>A
|
|
NM_001329603.1:c.-12-384T>A
|
NP_001316532.1:n.-12-384T>A
|
|
NR_138057.1:n.741+4028T>A
|
|
|
XM_006715376.3:c.-12-384T>A
|
XP_006715439.2:n.-12-384T>A
|
|
XM_011535550.2:c.-12-384T>A
|
XP_011533852.1:n.-12-384T>A
|
|
XM_011535552.3:c.-12+4703T>A
|
XP_011533854.1:n.-12+4703T>A
|
|
XM_011535553.3:c.-12+4028T>A
|
XP_011533855.1:n.-12+4028T>A
|
|
XM_011535554.2:c.-12-384T>A
|
XP_011533856.1:n.-12-384T>A
|
|
XM_011535555.2:c.-12-384T>A
|
XP_011533857.1:n.-12-384T>A
|
|
XM_011535556.3:c.-12-384T>A
|
XP_011533858.1:n.-12-384T>A
|
|
XM_011535559.3:c.-12-384T>A
|
XP_011533861.1:n.-12-384T>A
|
|
XM_017010384.1:c.-12-384T>A
|
XP_016865873.1:n.-12-384T>A
|
|
XM_017010385.2:c.-672+4703T>A
|
XP_016865874.1:n.-672+4703T>A
|
|
XM_017010386.1:c.-12-384T>A
|
XP_016865875.1:n.-12-384T>A
|
|
XM_017010387.2:c.-2068+4703T>A
|
XP_016865876.1:n.-2068+4703T>A
|
|
XM_017010388.2:c.-12-384T>A
|
XP_016865877.1:n.-12-384T>A
|
|
XM_024446350.1:c.-396T>A
|
XP_024302118.1:n.-396T>A
|
|
XR_942337.2:n.715-384T>A
|
|
|
NM_001145128.3:c.-12+4703T>A
MANE Select
|
NP_001138600.2:n.-12+4703T>A
|
|
NM_001329602.2:c.-12+4028T>A
|
NP_001316531.1:n.-12+4028T>A
|
|
NM_001329603.2:c.-12-384T>A
|
NP_001316532.1:n.-12-384T>A
|
|
NM_145025.5:c.-12+4703T>A
|
NP_659462.1:n.-12+4703T>A
|
|
NR_138057.2:n.731+4028T>A
|
|
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