ENST00000261304.7:c.680A>T
MANE Select
|
ENSP00000261304.2:p.Asp227Val
|
|
ENST00000261304.6:c.680A>T
|
ENSP00000261304.2:p.Asp227Val
|
|
ENST00000393568.8:c.611A>T
|
ENSP00000377198.4:p.Asp204Val
|
|
ENST00000393569.6:c.602A>T
|
ENSP00000377199.2:p.Asp201Val
|
|
ENST00000474294.6:n.670A>T
|
|
|
ENST00000477716.3:n.435A>T
|
|
|
ENST00000544807.6:c.512A>T
|
ENSP00000437513.2:p.Asp171Val
|
|
ENST00000554916.5:n.559A>T
|
|
|
ENST00000555000.5:c.47A>T
|
ENSP00000450472.1:p.Asp16Val
|
|
ENST00000557316.5:c.*78A>T
|
ENSP00000452314.1:n.*78A>T
|
|
ENST00000622264.4:c.670A>T
|
|
|
NM_000153.3:c.680A>T
|
NP_000144.2:p.Asp227Val
|
|
NM_001201401.1:c.611A>T
|
NP_001188330.1:p.Asp204Val
|
|
NM_001201402.1:c.602A>T
|
NP_001188331.1:p.Asp201Val
|
|
XM_011536618.1:c.512A>T
|
XP_011534920.1:p.Asp171Val
|
|
XM_011536618.2:c.512A>T
|
XP_011534920.1:p.Asp171Val
|
|
NM_000153.4:c.680A>T
MANE Select
|
NP_000144.2:p.Asp227Val
|
|
NM_001201401.2:c.611A>T
|
NP_001188330.1:p.Asp204Val
|
|
NM_001201402.2:c.602A>T
|
NP_001188331.1:p.Asp201Val
|
|