ENST00000264414.9:c.1207-409G>T
MANE Select
|
ENSP00000264414.4:n.1207-409G>T
|
|
ENST00000264414.8:c.1207-409G>T
|
ENSP00000264414.4:n.1207-409G>T
|
|
ENST00000344951.8:c.1009-409G>T
|
ENSP00000343601.4:n.1009-409G>T
|
|
ENST00000409096.5:c.1135-409G>T
|
ENSP00000387200.1:n.1135-409G>T
|
|
ENST00000409777.5:c.1135-409G>T
|
ENSP00000386525.1:n.1135-409G>T
|
|
ENST00000481135.1:n.94G>T
|
|
|
ENST00000617432.4:c.-70-409G>T
|
ENSP00000477851.1:n.-70-409G>T
|
|
NM_001257197.1:c.1009-409G>T
|
NP_001244126.1:n.1009-409G>T
|
|
NM_001257198.1:c.1225-409G>T
|
NP_001244127.1:n.1225-409G>T
|
|
NM_003590.4:c.1207-409G>T
|
NP_003581.1:n.1207-409G>T
|
|
XM_006712800.2:c.1174-409G>T
|
XP_006712863.2:n.1174-409G>T
|
|
XM_011511994.1:c.1060-409G>T
|
XP_011510296.1:n.1060-409G>T
|
|
XM_011511995.1:c.1165-409G>T
|
XP_011510297.1:n.1165-409G>T
|
|
XM_011511996.1:c.1015-409G>T
|
XP_011510298.1:n.1015-409G>T
|
|
XM_011511997.1:c.907-409G>T
|
XP_011510299.1:n.907-409G>T
|
|
XM_011511994.3:c.1060-409G>T
|
XP_011510296.1:n.1060-409G>T
|
|
XM_011511996.2:c.1015-409G>T
|
XP_011510298.1:n.1015-409G>T
|
|
NM_003590.5:c.1207-409G>T
MANE Select
|
NP_003581.1:n.1207-409G>T
|
|
NM_001257198.2:c.1225-409G>T
|
NP_001244127.1:n.1225-409G>T
|
|
NM_001257197.2:c.1009-409G>T
|
NP_001244126.1:n.1009-409G>T
|
|