ENST00000271651.8:c.588C>T
MANE Select
|
ENSP00000271651.3:p.Asp196=
|
|
ENST00000443913.2:c.765C>T
|
ENSP00000405083.2:p.Asp255=
|
|
ENST00000480670.2:n.3657C>T
|
|
|
ENST00000676680.1:c.588C>T
|
ENSP00000503270.1:p.Asp196=
|
|
ENST00000676716.1:c.465C>T
|
ENSP00000504737.1:p.Asp155=
|
|
ENST00000676751.1:c.588C>T
|
ENSP00000502964.1:p.Asp196=
|
|
ENST00000676824.1:c.588C>T
|
ENSP00000504176.1:p.Asp196=
|
|
ENST00000676966.1:c.588C>T
|
ENSP00000503723.1:p.Asp196=
|
|
ENST00000676970.1:c.588C>T
|
ENSP00000503832.1:p.Asp196=
|
|
ENST00000677330.1:n.2414C>T
|
|
|
ENST00000677611.1:n.440C>T
|
|
|
ENST00000677887.1:c.630C>T
|
ENSP00000503876.1:p.Asp210=
|
|
ENST00000678275.1:c.*480C>T
|
ENSP00000504796.1:n.*480C>T
|
|
ENST00000678337.1:c.624C>T
|
ENSP00000504759.1:p.Asp208=
|
|
ENST00000678725.1:n.1565C>T
|
|
|
ENST00000679090.1:n.1173C>T
|
|
|
ENST00000679148.1:n.3550C>T
|
|
|
ENST00000679171.1:n.2949C>T
|
|
|
ENST00000679260.1:c.399+1810C>T
|
ENSP00000504534.1:n.399+1810C>T
|
|
ENST00000271651.7:c.588C>T
|
ENSP00000271651.3:p.Asp196=
|
|
ENST00000443913.1:c.765C>T
|
ENSP00000405083.1:p.Asp255=
|
|
ENST00000480670.1:n.428C>T
|
|
|
NM_000396.3:c.588C>T
|
NP_000387.1:p.Asp196=
|
|
NM_000396.4:c.588C>T
MANE Select
|
NP_000387.1:p.Asp196=
|
|