ENST00000295897.9:c.1782G>C
MANE Select
|
ENSP00000295897.4:p.Glu594Asp
|
|
ENST00000295897.8:c.1782G>C
|
ENSP00000295897.4:p.Glu594Asp
|
|
ENST00000401494.7:c.1437G>C
|
ENSP00000384695.3:p.Glu479Asp
|
|
ENST00000415165.6:c.1206G>C
|
ENSP00000401820.2:p.Glu402Asp
|
|
ENST00000476441.6:c.*1061G>C
|
ENSP00000423727.1:n.*1061G>C
|
|
ENST00000495173.1:n.90G>C
|
|
|
ENST00000503124.5:c.1332G>C
|
ENSP00000421027.1:p.Glu444Asp
|
|
ENST00000505649.5:n.1329G>C
|
|
|
ENST00000508932.5:n.175+181G>C
|
|
|
ENST00000509063.5:c.1782G>C
|
ENSP00000422784.1:p.Glu594Asp
|
|
ENST00000511370.1:c.1315G>C
|
|
|
ENST00000621085.4:c.1143G>C
|
ENSP00000483421.1:p.Glu381Asp
|
|
ENST00000621628.4:c.1143G>C
|
ENSP00000480485.1:p.Glu381Asp
|
|
NM_000477.5:c.1782G>C
|
NP_000468.1:p.Glu594Asp
|
|
NM_000477.6:c.1782G>C
|
NP_000468.1:p.Glu594Asp
|
|
NM_000477.7:c.1782G>C
MANE Select
|
NP_000468.1:p.Glu594Asp
|
|