|
ENST00000700029.2:c.610_612delinsGCT
|
ENSP00000514759.2:p.Pro204Ala
|
|
|
ENST00000710265.1:c.610_612delinsGCT
|
ENSP00000518161.1:p.Pro204Ala
|
|
|
ENST00000472832.3:c.610_612delinsGCT
|
ENSP00000483066.2:p.Pro204Ala
|
|
|
ENST00000688158.2:n.1345_1347delinsGCT
|
|
|
|
ENST00000688922.2:c.*440_*442delinsGCT
|
ENSP00000508742.2:n.*440_*442delinsGCT
|
|
|
ENST00000700021.1:c.565_567delinsGCT
|
ENSP00000514757.1:p.Pro189Ala
|
|
|
ENST00000700022.1:c.493-5618_493-5616delinsGCT
|
ENSP00000514758.1:n.493-5618_493-5616delinsGCT
|
|
|
ENST00000700023.1:n.1768_1770delinsGCT
|
|
|
|
ENST00000700024.1:n.2002_2004delinsGCT
|
|
|
|
ENST00000700025.1:n.1379_1381delinsGCT
|
|
|
|
ENST00000700029.1:c.444_446delinsGCT
|
|
|
|
ENST00000706954.1:c.610_612delinsGCT
|
ENSP00000516674.1:p.Pro204Ala
|
|
|
ENST00000706955.1:c.*645_*647delinsGCT
|
ENSP00000516675.1:n.*645_*647delinsGCT
|
|
|
ENST00000686459.1:c.*196_*198delinsGCT
|
ENSP00000508909.1:n.*196_*198delinsGCT
|
|
|
ENST00000688158.1:c.*721_*723delinsGCT
|
ENSP00000509254.1:n.*721_*723delinsGCT
|
|
|
ENST00000688308.1:c.610_612delinsGCT
|
ENSP00000508752.1:p.Pro204Ala
|
|
|
ENST00000688922.1:c.531_533delinsGCT
|
|
|
|
ENST00000693560.1:c.1129_1131delinsGCT
|
ENSP00000509861.1:p.Pro377Ala
|
|
|
ENST00000371953.8:c.610_612delinsGCT
MANE Select
|
ENSP00000361021.3:p.Pro204Ala
|
|
|
ENST00000371953.7:c.610_612delinsGCT
|
ENSP00000361021.3:p.Pro204Ala
|
|
|
ENST00000472832.2:c.37_39delinsGCT
|
ENSP00000483066.1:p.Pro13Ala
|
|
|
NM_000314.5:c.610_612delinsGCT
|
NP_000305.3:p.Pro204Ala
|
|
|
NM_000314.6:c.610_612delinsGCT
|
NP_000305.3:p.Pro204Ala
|
|
|
NM_001304717.2:c.1129_1131delinsGCT
|
NP_001291646.2:p.Pro377Ala
|
|
|
NM_001304718.1:c.19_21delinsGCT
|
NP_001291647.1:p.Pro7Ala
|
|
|
XM_006717926.2:c.565_567delinsGCT
|
XP_006717989.1:p.Pro189Ala
|
|
|
XM_011539981.1:c.610_612delinsGCT
|
XP_011538283.1:p.Pro204Ala
|
|
|
XM_011539982.1:c.514_516delinsGCT
|
XP_011538284.1:p.Pro172Ala
|
|
|
XR_945791.1:n.1205-5618_1205-5616delinsGCT
|
|
|
|
NM_000314.7:c.610_612delinsGCT
|
NP_000305.3:p.Pro204Ala
|
|
|
NM_001304717.5:c.1129_1131delinsGCT
|
NP_001291646.4:p.Pro377Ala
|
|
|
NM_001304718.2:c.19_21delinsGCT
|
NP_001291647.1:p.Pro7Ala
|
|
|
NM_000314.8:c.610_612delinsGCT
MANE Select
|
NP_000305.3:p.Pro204Ala
|
|
