|
ENST00000700029.2:c.769_771delinsGCT
|
ENSP00000514759.2:p.Phe257Ala
|
|
|
ENST00000710265.1:c.769_771delinsGCT
|
ENSP00000518161.1:p.Phe257Ala
|
|
|
ENST00000472832.3:c.769_771delinsGCT
|
ENSP00000483066.2:p.Phe257Ala
|
|
|
ENST00000688158.2:n.1504_1506delinsGCT
|
|
|
|
ENST00000688922.2:c.*599_*601delinsGCT
|
ENSP00000508742.2:n.*599_*601delinsGCT
|
|
|
ENST00000700021.1:c.724_726delinsGCT
|
ENSP00000514757.1:p.Phe242Ala
|
|
|
ENST00000700022.1:c.*108_*110delinsGCT
|
ENSP00000514758.1:n.*108_*110delinsGCT
|
|
|
ENST00000700023.1:n.1927_1929delinsGCT
|
|
|
|
ENST00000700024.1:n.2161_2163delinsGCT
|
|
|
|
ENST00000700025.1:n.1538_1540delinsGCT
|
|
|
|
ENST00000700026.1:n.406_408delinsGCT
|
|
|
|
ENST00000700029.1:c.603_605delinsGCT
|
|
|
|
ENST00000706954.1:c.769_771delinsGCT
|
ENSP00000516674.1:p.Phe257Ala
|
|
|
ENST00000706955.1:c.*804_*806delinsGCT
|
ENSP00000516675.1:n.*804_*806delinsGCT
|
|
|
ENST00000686459.1:c.*355_*357delinsGCT
|
ENSP00000508909.1:n.*355_*357delinsGCT
|
|
|
ENST00000688158.1:c.*880_*882delinsGCT
|
ENSP00000509254.1:n.*880_*882delinsGCT
|
|
|
ENST00000688308.1:c.769_771delinsGCT
|
ENSP00000508752.1:p.Phe257Ala
|
|
|
ENST00000688922.1:c.690_692delinsGCT
|
|
|
|
ENST00000693560.1:c.1288_1290delinsGCT
|
ENSP00000509861.1:p.Phe430Ala
|
|
|
ENST00000371953.8:c.769_771delinsGCT
MANE Select
|
ENSP00000361021.3:p.Phe257Ala
|
|
|
ENST00000371953.7:c.769_771delinsGCT
|
ENSP00000361021.3:p.Phe257Ala
|
|
|
ENST00000472832.2:c.196_198delinsGCT
|
ENSP00000483066.1:p.Phe66Ala
|
|
|
NM_000314.5:c.769_771delinsGCT
|
NP_000305.3:p.Phe257Ala
|
|
|
NM_000314.6:c.769_771delinsGCT
|
NP_000305.3:p.Phe257Ala
|
|
|
NM_001304717.2:c.1288_1290delinsGCT
|
NP_001291646.2:p.Phe430Ala
|
|
|
NM_001304718.1:c.178_180delinsGCT
|
NP_001291647.1:p.Phe60Ala
|
|
|
XM_006717926.2:c.724_726delinsGCT
|
XP_006717989.1:p.Phe242Ala
|
|
|
XM_011539981.1:c.769_771delinsGCT
|
XP_011538283.1:p.Phe257Ala
|
|
|
XM_011539982.1:c.673_675delinsGCT
|
XP_011538284.1:p.Phe225Ala
|
|
|
XR_945791.1:n.1339_1341delinsGCT
|
|
|
|
NM_000314.7:c.769_771delinsGCT
|
NP_000305.3:p.Phe257Ala
|
|
|
NM_001304717.5:c.1288_1290delinsGCT
|
NP_001291646.4:p.Phe430Ala
|
|
|
NM_001304718.2:c.178_180delinsGCT
|
NP_001291647.1:p.Phe60Ala
|
|
|
NM_000314.8:c.769_771delinsGCT
MANE Select
|
NP_000305.3:p.Phe257Ala
|
|
