ENST00000261304.7:c.696C>T
MANE Select
|
ENSP00000261304.2:p.Ser232=
|
|
ENST00000261304.6:c.696C>T
|
ENSP00000261304.2:p.Ser232=
|
|
ENST00000393568.8:c.627C>T
|
ENSP00000377198.4:p.Ser209=
|
|
ENST00000393569.6:c.618C>T
|
ENSP00000377199.2:p.Ser206=
|
|
ENST00000474294.6:n.686C>T
|
|
|
ENST00000477716.3:n.451C>T
|
|
|
ENST00000544807.6:c.528C>T
|
ENSP00000437513.2:p.Ser176=
|
|
ENST00000554916.5:n.575C>T
|
|
|
ENST00000555000.5:c.63C>T
|
ENSP00000450472.1:p.Ser21=
|
|
ENST00000557316.5:c.*94C>T
|
ENSP00000452314.1:n.*94C>T
|
|
ENST00000622264.4:c.686C>T
|
|
|
NM_000153.3:c.696C>T
|
NP_000144.2:p.Ser232=
|
|
NM_001201401.1:c.627C>T
|
NP_001188330.1:p.Ser209=
|
|
NM_001201402.1:c.618C>T
|
NP_001188331.1:p.Ser206=
|
|
XM_011536618.1:c.528C>T
|
XP_011534920.1:p.Ser176=
|
|
XM_011536618.2:c.528C>T
|
XP_011534920.1:p.Ser176=
|
|
NM_000153.4:c.696C>T
MANE Select
|
NP_000144.2:p.Ser232=
|
|
NM_001201401.2:c.627C>T
|
NP_001188330.1:p.Ser209=
|
|
NM_001201402.2:c.618C>T
|
NP_001188331.1:p.Ser206=
|
|