|
ENST00000457416.7:c.*449dup
MANE Plus Clinical
|
ENSP00000410294.2:n.*449dup
|
|
|
ENST00000351936.11:c.*449dup
|
ENSP00000309878.10:n.*449dup
|
|
|
ENST00000638709.2:c.*449dup
|
ENSP00000491912.2:n.*449dup
|
|
|
ENST00000682296.1:n.2257dup
|
|
|
|
ENST00000682550.1:c.*449dup
|
ENSP00000507633.1:n.*449dup
|
|
|
ENST00000682772.1:c.*449dup
|
ENSP00000506848.1:n.*449dup
|
|
|
ENST00000682904.1:n.1735dup
|
|
|
|
ENST00000683029.1:n.2918dup
|
|
|
|
ENST00000683211.1:c.*449dup
|
ENSP00000508257.1:n.*449dup
|
|
|
ENST00000683250.1:c.*3208dup
|
ENSP00000506847.1:n.*3208dup
|
|
|
ENST00000683418.1:n.5256dup
|
|
|
|
ENST00000684153.1:c.*643dup
|
ENSP00000506937.1:n.*643dup
|
|
|
ENST00000684516.1:n.3928dup
|
|
|
|
ENST00000358487.10:c.*449dup
MANE Select
|
ENSP00000351276.6:n.*449dup
|
|
|
ENST00000638709.1:c.902dup
|
|
|
|
ENST00000356226.8:c.*449dup
|
ENSP00000348559.4:n.*449dup
|
|
|
ENST00000357555.9:c.*173dup
|
ENSP00000350166.5:n.*173dup
|
|
|
ENST00000358487.9:c.*449dup
|
ENSP00000351276.5:n.*449dup
|
|
|
ENST00000369060.8:c.*449dup
|
ENSP00000358056.4:n.*449dup
|
|
|
ENST00000369061.8:c.*449dup
|
ENSP00000358057.4:n.*449dup
|
|
|
ENST00000478859.5:c.*449dup
|
ENSP00000474011.1:n.*449dup
|
|
|
ENST00000604236.5:c.*1962dup
|
ENSP00000474109.1:n.*1962dup
|
|
|
ENST00000613048.4:c.*449dup
|
ENSP00000484154.1:n.*449dup
|
|
|
NM_000141.4:c.*449dup
|
NP_000132.3:n.*449dup
|
|
|
NM_001144914.1:c.*449dup
|
NP_001138386.1:n.*449dup
|
|
|
NM_001144915.1:c.*173dup
|
NP_001138387.1:n.*173dup
|
|
|
NM_001144916.1:c.*449dup
|
NP_001138388.1:n.*449dup
|
|
|
NM_001144917.1:c.*449dup
|
NP_001138389.1:n.*449dup
|
|
|
NM_001144918.1:c.*449dup
|
NP_001138390.1:n.*449dup
|
|
|
NM_022970.3:c.*449dup
|
NP_075259.4:n.*449dup
|
|
|
NM_023029.2:c.*449dup
|
NP_075418.1:n.*449dup
|
|
|
NR_073009.1:n.3365dup
|
|
|
|
XM_006717708.2:c.*449dup
|
XP_006717771.1:n.*449dup
|
|
|
XM_006717709.2:c.*449dup
|
XP_006717772.1:n.*449dup
|
|
|
XM_006717711.2:c.*449dup
|
XP_006717774.1:n.*449dup
|
|
|
XM_006717712.2:c.*449dup
|
XP_006717775.1:n.*449dup
|
|
|
XM_011539510.1:c.*449dup
|
XP_011537812.1:n.*449dup
|
|
|
NM_001320654.1:c.*449dup
|
NP_001307583.1:n.*449dup
|
|
|
NM_001320658.1:c.*449dup
|
NP_001307587.1:n.*449dup
|
|
|
XM_006717708.3:c.*449dup
|
XP_006717771.1:n.*449dup
|
|
|
XM_006717710.4:c.*643dup
|
XP_006717773.1:n.*643dup
|
|
|
XM_017015920.2:c.*643dup
|
XP_016871409.1:n.*643dup
|
|
|
XM_017015921.2:c.*643dup
|
XP_016871410.1:n.*643dup
|
|
|
XM_017015924.2:c.*449dup
|
XP_016871413.1:n.*449dup
|
|
|
XM_017015925.2:c.*643dup
|
XP_016871414.1:n.*643dup
|
|
|
XM_024447887.1:c.*449dup
|
XP_024303655.1:n.*449dup
|
|
|
XM_024447888.1:c.*449dup
|
XP_024303656.1:n.*449dup
|
|
|
XM_024447889.1:c.*449dup
|
XP_024303657.1:n.*449dup
|
|
|
XM_024447890.1:c.*449dup
|
XP_024303658.1:n.*449dup
|
|
|
XM_024447891.1:c.*449dup
|
XP_024303659.1:n.*449dup
|
|
|
XM_024447892.1:c.*449dup
|
XP_024303660.1:n.*449dup
|
|
|
NM_000141.5:c.*449dup
MANE Select
|
NP_000132.3:n.*449dup
|
|
|
NM_001144917.2:c.*449dup
|
NP_001138389.1:n.*449dup
|
|
|
NM_001144918.2:c.*449dup
|
NP_001138390.1:n.*449dup
|
|
|
NM_001320658.2:c.*449dup
|
NP_001307587.1:n.*449dup
|
|
|
NR_073009.2:n.3351dup
|
|
|
|
NM_001144915.2:c.*173dup
|
NP_001138387.1:n.*173dup
|
|
|
NM_001144916.2:c.*449dup
|
NP_001138388.1:n.*449dup
|
|
|
NM_001320654.2:c.*449dup
|
NP_001307583.1:n.*449dup
|
|
