ENST00000234071.8:c.1028del
MANE Select
|
ENSP00000234071.4:p.Gly343AlafsTer?
|
|
ENST00000234071.7:c.1028del
|
ENSP00000234071.3:p.Gly343AlafsTer?
|
|
ENST00000402125.2:c.352del
|
|
|
ENST00000409048.1:c.1130del
|
ENSP00000386679.1:p.Gly377AlafsTer?
|
|
NM_000312.3:c.1028del , LRG_599t1:c.1028del
|
NP_000303.1:p.Gly343AlafsTer?
|
|
XM_005263715.3:c.1211del
|
XP_005263772.1:p.Gly404AlafsTer?
|
|
XM_005263716.3:c.1193del
|
XP_005263773.1:p.Gly398AlafsTer?
|
|
XM_005263717.3:c.1091del
|
XP_005263774.1:p.Gly364AlafsTer?
|
|
XR_923313.1:n.1332-321del
|
|
|
XM_005263717.4:c.1091del
|
XP_005263774.1:p.Gly364AlafsTer?
|
|
XM_017004505.1:c.1271del
|
XP_016859994.1:p.Gly424AlafsTer?
|
|
XM_024453002.1:c.1373del
|
XP_024308770.1:p.Gly458AlafsTer?
|
|
XM_024453003.1:c.1313del
|
XP_024308771.1:p.Gly438AlafsTer?
|
|
XM_024453004.1:c.1211del
|
XP_024308772.1:p.Gly404AlafsTer?
|
|
XM_024453005.1:c.1193del
|
XP_024308773.1:p.Gly398AlafsTer?
|
|
XM_024453006.1:c.1130del
|
XP_024308774.1:p.Gly377AlafsTer?
|
|
XR_001739705.1:n.3607-321del
|
|
|
XR_923313.2:n.4043-321del
|
|
|
NM_000312.4:c.1028del
MANE Select
|
NP_000303.1:p.Gly343AlafsTer?
|
|
NM_001375602.1:c.1211del
|
NP_001362531.1:p.Gly404AlafsTer?
|
|
NM_001375603.1:c.1193del
|
NP_001362532.1:p.Gly398AlafsTer?
|
|
NM_001375604.1:c.1091del
|
NP_001362533.1:p.Gly364AlafsTer?
|
|
NM_001375605.1:c.1130del
|
NP_001362534.1:p.Gly377AlafsTer?
|
|
NM_001375606.1:c.1196del
|
NP_001362535.1:p.Gly399AlafsTer?
|
|
NM_001375607.1:c.1214del
|
NP_001362536.1:p.Gly405AlafsTer?
|
|
NM_001375608.1:c.971del
|
NP_001362537.1:p.Gly324AlafsTer?
|
|
NM_001375609.1:c.1004del
|
NP_001362538.1:p.Gly335AlafsTer?
|
|
NM_001375610.1:c.1022del
|
NP_001362539.1:p.Gly341AlafsTer?
|
|
NM_001375611.1:c.1028del
|
NP_001362540.1:p.Gly343AlafsTer?
|
|
NM_001375613.1:c.1028del
|
NP_001362542.1:p.Gly343AlafsTer?
|
|