|
ENST00000700029.2:c.727_729delinsGTT
|
ENSP00000514759.2:p.Phe243Val
|
|
|
ENST00000710265.1:c.727_729delinsGTT
|
ENSP00000518161.1:p.Phe243Val
|
|
|
ENST00000472832.3:c.727_729delinsGTT
|
ENSP00000483066.2:p.Phe243Val
|
|
|
ENST00000688158.2:n.1462_1464delinsGTT
|
|
|
|
ENST00000688922.2:c.*557_*559delinsGTT
|
ENSP00000508742.2:n.*557_*559delinsGTT
|
|
|
ENST00000700021.1:c.682_684delinsGTT
|
ENSP00000514757.1:p.Phe228Val
|
|
|
ENST00000700022.1:c.*66_*68delinsGTT
|
ENSP00000514758.1:n.*66_*68delinsGTT
|
|
|
ENST00000700023.1:n.1885_1887delinsGTT
|
|
|
|
ENST00000700024.1:n.2119_2121delinsGTT
|
|
|
|
ENST00000700025.1:n.1496_1498delinsGTT
|
|
|
|
ENST00000700026.1:n.364_366delinsGTT
|
|
|
|
ENST00000700029.1:c.561_563delinsGTT
|
|
|
|
ENST00000706954.1:c.727_729delinsGTT
|
ENSP00000516674.1:p.Phe243Val
|
|
|
ENST00000706955.1:c.*762_*764delinsGTT
|
ENSP00000516675.1:n.*762_*764delinsGTT
|
|
|
ENST00000686459.1:c.*313_*315delinsGTT
|
ENSP00000508909.1:n.*313_*315delinsGTT
|
|
|
ENST00000688158.1:c.*838_*840delinsGTT
|
ENSP00000509254.1:n.*838_*840delinsGTT
|
|
|
ENST00000688308.1:c.727_729delinsGTT
|
ENSP00000508752.1:p.Phe243Val
|
|
|
ENST00000688922.1:c.648_650delinsGTT
|
|
|
|
ENST00000693560.1:c.1246_1248delinsGTT
|
ENSP00000509861.1:p.Phe416Val
|
|
|
ENST00000371953.8:c.727_729delinsGTT
MANE Select
|
ENSP00000361021.3:p.Phe243Val
|
|
|
ENST00000371953.7:c.727_729delinsGTT
|
ENSP00000361021.3:p.Phe243Val
|
|
|
ENST00000472832.2:c.154_156delinsGTT
|
ENSP00000483066.1:p.Phe52Val
|
|
|
NM_000314.5:c.727_729delinsGTT
|
NP_000305.3:p.Phe243Val
|
|
|
NM_000314.6:c.727_729delinsGTT
|
NP_000305.3:p.Phe243Val
|
|
|
NM_001304717.2:c.1246_1248delinsGTT
|
NP_001291646.2:p.Phe416Val
|
|
|
NM_001304718.1:c.136_138delinsGTT
|
NP_001291647.1:p.Phe46Val
|
|
|
XM_006717926.2:c.682_684delinsGTT
|
XP_006717989.1:p.Phe228Val
|
|
|
XM_011539981.1:c.727_729delinsGTT
|
XP_011538283.1:p.Phe243Val
|
|
|
XM_011539982.1:c.631_633delinsGTT
|
XP_011538284.1:p.Phe211Val
|
|
|
XR_945791.1:n.1297_1299delinsGTT
|
|
|
|
NM_000314.7:c.727_729delinsGTT
|
NP_000305.3:p.Phe243Val
|
|
|
NM_001304717.5:c.1246_1248delinsGTT
|
NP_001291646.4:p.Phe416Val
|
|
|
NM_001304718.2:c.136_138delinsGTT
|
NP_001291647.1:p.Phe46Val
|
|
|
NM_000314.8:c.727_729delinsGTT
MANE Select
|
NP_000305.3:p.Phe243Val
|
|
