ENST00000346342.8:c.1325dup
MANE Select
|
ENSP00000329546.4:p.Phe443IlefsTer?
|
|
ENST00000346342.7:c.1325dup
|
ENSP00000329546.3:p.Phe443IlefsTer?
|
|
ENST00000375581.3:c.1391dup
|
ENSP00000364731.3:p.Phe465IlefsTer?
|
|
ENST00000541084.5:c.1139dup
|
ENSP00000442051.2:p.Phe381IlefsTer?
|
|
NM_000131.4:c.1391dup , LRG_554t1:c.1391dup
|
NP_000122.1:p.Phe465IlefsTer?
|
|
NM_001267554.1:c.1139dup
|
NP_001254483.1:p.Phe381IlefsTer?
|
|
NM_019616.3:c.1325dup , LRG_554t2:c.1325dup
|
NP_062562.1:p.Phe443IlefsTer?
|
|
NR_051961.1:n.1412dup
|
|
|
XM_006719963.2:c.1184dup
|
XP_006720026.1:p.Phe396IlefsTer?
|
|
XM_011537474.1:c.1433dup
|
XP_011535776.1:p.Phe479IlefsTer?
|
|
XM_011537475.1:c.1247dup
|
XP_011535777.1:p.Phe417IlefsTer?
|
|
XM_011537476.1:c.1085dup
|
XP_011535778.1:p.Phe363IlefsTer?
|
|
XM_011537477.1:c.1394dup
|
XP_011535779.1:p.Phe466IlefsTer?
|
|
XM_006719963.3:c.1229dup
|
XP_006720026.2:p.Phe411IlefsTer?
|
|
XM_011537474.2:c.1478dup
|
XP_011535776.2:p.Phe494IlefsTer?
|
|
XM_011537475.2:c.1292dup
|
XP_011535777.2:p.Phe432IlefsTer?
|
|
XM_011537476.2:c.1085dup
|
XP_011535778.1:p.Phe363IlefsTer?
|
|
NM_019616.4:c.1325dup
MANE Select
|
NP_062562.1:p.Phe443IlefsTer?
|
|
NR_051961.2:n.1409dup
|
|
|
NM_001267554.2:c.1139dup
|
NP_001254483.1:p.Phe381IlefsTer?
|
|