ENST00000261304.7:c.843T>C
MANE Select
|
ENSP00000261304.2:p.Ser281=
|
|
ENST00000261304.6:c.843T>C
|
ENSP00000261304.2:p.Ser281=
|
|
ENST00000393568.8:c.774T>C
|
ENSP00000377198.4:p.Ser258=
|
|
ENST00000393569.6:c.765T>C
|
ENSP00000377199.2:p.Ser255=
|
|
ENST00000474294.6:n.833T>C
|
|
|
ENST00000477716.3:n.598T>C
|
|
|
ENST00000544807.6:c.675T>C
|
ENSP00000437513.2:p.Ser225=
|
|
ENST00000555000.5:c.210T>C
|
ENSP00000450472.1:p.Ser70=
|
|
ENST00000557316.5:c.*241T>C
|
ENSP00000452314.1:n.*241T>C
|
|
ENST00000622264.4:c.833T>C
|
|
|
NM_000153.3:c.843T>C
|
NP_000144.2:p.Ser281=
|
|
NM_001201401.1:c.774T>C
|
NP_001188330.1:p.Ser258=
|
|
NM_001201402.1:c.765T>C
|
NP_001188331.1:p.Ser255=
|
|
XM_011536618.1:c.675T>C
|
XP_011534920.1:p.Ser225=
|
|
XM_011536618.2:c.675T>C
|
XP_011534920.1:p.Ser225=
|
|
NM_000153.4:c.843T>C
MANE Select
|
NP_000144.2:p.Ser281=
|
|
NM_001201401.2:c.774T>C
|
NP_001188330.1:p.Ser258=
|
|
NM_001201402.2:c.765T>C
|
NP_001188331.1:p.Ser255=
|
|