ENST00000553106.6:c.1056_1057delinsTG
MANE Select
|
ENSP00000448059.1:p.Gly352=
|
|
ENST00000307000.7:c.1041_1042delinsTG
|
ENSP00000303500.2:p.Gly347=
|
|
ENST00000549247.6:n.815_816delinsTG
|
|
|
ENST00000551114.2:n.718_719delinsTG
|
|
|
ENST00000553106.5:c.1056_1057delinsTG
|
ENSP00000448059.1:p.Gly352=
|
|
ENST00000635477.1:c.160_161delinsTG
|
|
|
ENST00000635528.1:n.571_572delinsTG
|
|
|
NM_000277.1:c.1056_1057delinsTG
|
NP_000268.1:p.Gly352=
|
|
XM_011538422.1:c.999_1000delinsTG
|
XP_011536724.1:p.Gly333=
|
|
NM_000277.2:c.1056_1057delinsTG
|
NP_000268.1:p.Gly352=
|
|
NM_001354304.1:c.1056_1057delinsTG
|
NP_001341233.1:p.Gly352=
|
|
NM_000277.3:c.1056_1057delinsTG
MANE Select
|
NP_000268.1:p.Gly352=
|
|
NM_001354304.2:c.1056_1057delinsTG
|
NP_001341233.1:p.Gly352=
|
|