ENST00000261304.7:c.702T>C
MANE Select
|
ENSP00000261304.2:p.Ser234=
|
|
ENST00000261304.6:c.702T>C
|
ENSP00000261304.2:p.Ser234=
|
|
ENST00000393568.8:c.633T>C
|
ENSP00000377198.4:p.Ser211=
|
|
ENST00000393569.6:c.624T>C
|
ENSP00000377199.2:p.Ser208=
|
|
ENST00000474294.6:n.692T>C
|
|
|
ENST00000477716.3:n.457T>C
|
|
|
ENST00000544807.6:c.534T>C
|
ENSP00000437513.2:p.Ser178=
|
|
ENST00000554916.5:n.581T>C
|
|
|
ENST00000555000.5:c.69T>C
|
ENSP00000450472.1:p.Ser23=
|
|
ENST00000557316.5:c.*100T>C
|
ENSP00000452314.1:n.*100T>C
|
|
ENST00000622264.4:c.692T>C
|
|
|
NM_000153.3:c.702T>C
|
NP_000144.2:p.Ser234=
|
|
NM_001201401.1:c.633T>C
|
NP_001188330.1:p.Ser211=
|
|
NM_001201402.1:c.624T>C
|
NP_001188331.1:p.Ser208=
|
|
XM_011536618.1:c.534T>C
|
XP_011534920.1:p.Ser178=
|
|
XM_011536618.2:c.534T>C
|
XP_011534920.1:p.Ser178=
|
|
NM_000153.4:c.702T>C
MANE Select
|
NP_000144.2:p.Ser234=
|
|
NM_001201401.2:c.633T>C
|
NP_001188330.1:p.Ser211=
|
|
NM_001201402.2:c.624T>C
|
NP_001188331.1:p.Ser208=
|
|