ENST00000261304.7:c.905C>A
MANE Select
|
ENSP00000261304.2:p.Thr302Asn
|
|
ENST00000261304.6:c.905C>A
|
ENSP00000261304.2:p.Thr302Asn
|
|
ENST00000393568.8:c.836C>A
|
ENSP00000377198.4:p.Thr279Asn
|
|
ENST00000393569.6:c.827C>A
|
ENSP00000377199.2:p.Thr276Asn
|
|
ENST00000474294.6:n.895C>A
|
|
|
ENST00000544807.6:c.737C>A
|
ENSP00000437513.2:p.Thr246Asn
|
|
ENST00000555000.5:c.272C>A
|
ENSP00000450472.1:p.Thr91Asn
|
|
ENST00000557316.5:c.*303C>A
|
ENSP00000452314.1:n.*303C>A
|
|
ENST00000622264.4:c.895C>A
|
|
|
NM_000153.3:c.905C>A
|
NP_000144.2:p.Thr302Asn
|
|
NM_001201401.1:c.836C>A
|
NP_001188330.1:p.Thr279Asn
|
|
NM_001201402.1:c.827C>A
|
NP_001188331.1:p.Thr276Asn
|
|
XM_011536618.1:c.737C>A
|
XP_011534920.1:p.Thr246Asn
|
|
XM_011536618.2:c.737C>A
|
XP_011534920.1:p.Thr246Asn
|
|
NM_000153.4:c.905C>A
MANE Select
|
NP_000144.2:p.Thr302Asn
|
|
NM_001201401.2:c.836C>A
|
NP_001188330.1:p.Thr279Asn
|
|
NM_001201402.2:c.827C>A
|
NP_001188331.1:p.Thr276Asn
|
|