|
ENST00000357060.8:c.3374_3375delinsGA
MANE Select
|
ENSP00000349568.3:p.Gly1125=
|
|
|
ENST00000357060.7:c.3374_3375delinsGA
|
ENSP00000349568.3:p.Gly1125=
|
|
|
ENST00000434629.5:c.1456_1457delinsGA
|
|
|
|
NM_025145.5:c.3374_3375delinsGA
|
NP_079421.5:p.Gly1125=
|
|
|
XM_005270171.1:c.3377_3378delinsGA
|
XP_005270228.1:p.Gly1126=
|
|
|
XM_005270172.2:c.3377_3378delinsGA
|
XP_005270229.1:p.Gly1126=
|
|
|
XM_011540196.1:c.3491_3492delinsGA
|
XP_011538498.1:p.Gly1164=
|
|
|
XM_011540197.1:c.3491_3492delinsGA
|
XP_011538499.1:p.Gly1164=
|
|
|
XM_011540198.1:c.3374_3375delinsGA
|
XP_011538500.1:p.Gly1125=
|
|
|
XM_011540199.1:c.3374_3375delinsGA
|
XP_011538501.1:p.Gly1125=
|
|
|
XM_011540200.1:c.3491_3492delinsGA
|
XP_011538502.1:p.Gly1164=
|
|
|
XM_011540201.1:c.3491_3492delinsGA
|
XP_011538503.1:p.Gly1164=
|
|
|
XM_011540202.1:c.2720_2721delinsGA
|
XP_011538504.1:p.Gly907=
|
|
|
XM_011540203.1:c.1274_1275delinsGA
|
XP_011538505.1:p.Gly425=
|
|
|
NM_025145.6:c.3374_3375delinsGA
|
NP_079421.5:p.Gly1125=
|
|
|
XM_005270171.2:c.3377_3378delinsGA
|
XP_005270228.1:p.Gly1126=
|
|
|
XM_005270172.3:c.3377_3378delinsGA
|
XP_005270229.1:p.Gly1126=
|
|
|
XM_011540196.2:c.3491_3492delinsGA
|
XP_011538498.1:p.Gly1164=
|
|
|
XM_011540197.2:c.3491_3492delinsGA
|
XP_011538499.1:p.Gly1164=
|
|
|
XM_011540198.2:c.3374_3375delinsGA
|
XP_011538500.1:p.Gly1125=
|
|
|
XM_011540199.2:c.3374_3375delinsGA
|
XP_011538501.1:p.Gly1125=
|
|
|
XM_011540200.2:c.3491_3492delinsGA
|
XP_011538502.1:p.Gly1164=
|
|
|
XM_011540201.2:c.3491_3492delinsGA
|
XP_011538503.1:p.Gly1164=
|
|
|
XM_011540202.2:c.2720_2721delinsGA
|
XP_011538504.1:p.Gly907=
|
|
|
XM_017016681.1:c.3488_3489delinsGA
|
XP_016872170.1:p.Gly1163=
|
|
|
XM_017016682.1:c.3143_3144delinsGA
|
XP_016872171.1:p.Gly1048=
|
|
|
XM_024448177.1:c.1877_1878delinsGA
|
XP_024303945.1:p.Gly626=
|
|
|
XM_024448178.1:c.1274_1275delinsGA
|
XP_024303946.1:p.Gly425=
|
|
|
XR_002957015.1:n.3260_3261delinsGA
|
|
|
|
NM_025145.7:c.3374_3375delinsGA
MANE Select
|
NP_079421.5:p.Gly1125=
|
|
