|
ENST00000700029.2:c.778_780delinsGCT
|
ENSP00000514759.2:p.Lys260Ala
|
|
|
ENST00000710265.1:c.778_780delinsGCT
|
ENSP00000518161.1:p.Lys260Ala
|
|
|
ENST00000472832.3:c.778_780delinsGCT
|
ENSP00000483066.2:p.Lys260Ala
|
|
|
ENST00000688158.2:n.1513_1515delinsGCT
|
|
|
|
ENST00000688922.2:c.*608_*610delinsGCT
|
ENSP00000508742.2:n.*608_*610delinsGCT
|
|
|
ENST00000700021.1:c.733_735delinsGCT
|
ENSP00000514757.1:p.Lys245Ala
|
|
|
ENST00000700022.1:c.*117_*119delinsGCT
|
ENSP00000514758.1:n.*117_*119delinsGCT
|
|
|
ENST00000700023.1:n.1936_1938delinsGCT
|
|
|
|
ENST00000700024.1:n.2170_2172delinsGCT
|
|
|
|
ENST00000700025.1:n.1547_1549delinsGCT
|
|
|
|
ENST00000700026.1:n.415_417delinsGCT
|
|
|
|
ENST00000700029.1:c.612_614delinsGCT
|
|
|
|
ENST00000706954.1:c.778_780delinsGCT
|
ENSP00000516674.1:p.Lys260Ala
|
|
|
ENST00000706955.1:c.*813_*815delinsGCT
|
ENSP00000516675.1:n.*813_*815delinsGCT
|
|
|
ENST00000686459.1:c.*364_*366delinsGCT
|
ENSP00000508909.1:n.*364_*366delinsGCT
|
|
|
ENST00000688158.1:c.*889_*891delinsGCT
|
ENSP00000509254.1:n.*889_*891delinsGCT
|
|
|
ENST00000688308.1:c.778_780delinsGCT
|
ENSP00000508752.1:p.Lys260Ala
|
|
|
ENST00000688922.1:c.699_701delinsGCT
|
|
|
|
ENST00000693560.1:c.1297_1299delinsGCT
|
ENSP00000509861.1:p.Lys433Ala
|
|
|
ENST00000371953.8:c.778_780delinsGCT
MANE Select
|
ENSP00000361021.3:p.Lys260Ala
|
|
|
ENST00000371953.7:c.778_780delinsGCT
|
ENSP00000361021.3:p.Lys260Ala
|
|
|
ENST00000472832.2:c.205_207delinsGCT
|
ENSP00000483066.1:p.Lys69Ala
|
|
|
NM_000314.5:c.778_780delinsGCT
|
NP_000305.3:p.Lys260Ala
|
|
|
NM_000314.6:c.778_780delinsGCT
|
NP_000305.3:p.Lys260Ala
|
|
|
NM_001304717.2:c.1297_1299delinsGCT
|
NP_001291646.2:p.Lys433Ala
|
|
|
NM_001304718.1:c.187_189delinsGCT
|
NP_001291647.1:p.Lys63Ala
|
|
|
XM_006717926.2:c.733_735delinsGCT
|
XP_006717989.1:p.Lys245Ala
|
|
|
XM_011539981.1:c.778_780delinsGCT
|
XP_011538283.1:p.Lys260Ala
|
|
|
XM_011539982.1:c.682_684delinsGCT
|
XP_011538284.1:p.Lys228Ala
|
|
|
XR_945791.1:n.1348_1350delinsGCT
|
|
|
|
NM_000314.7:c.778_780delinsGCT
|
NP_000305.3:p.Lys260Ala
|
|
|
NM_001304717.5:c.1297_1299delinsGCT
|
NP_001291646.4:p.Lys433Ala
|
|
|
NM_001304718.2:c.187_189delinsGCT
|
NP_001291647.1:p.Lys63Ala
|
|
|
NM_000314.8:c.778_780delinsGCT
MANE Select
|
NP_000305.3:p.Lys260Ala
|
|
