ENST00000295897.9:c.1767G>C
MANE Select
|
ENSP00000295897.4:p.Glu589Asp
|
|
ENST00000295897.8:c.1767G>C
|
ENSP00000295897.4:p.Glu589Asp
|
|
ENST00000401494.7:c.1422G>C
|
ENSP00000384695.3:p.Glu474Asp
|
|
ENST00000415165.6:c.1191G>C
|
ENSP00000401820.2:p.Glu397Asp
|
|
ENST00000476441.6:c.*1046G>C
|
ENSP00000423727.1:n.*1046G>C
|
|
ENST00000495173.1:n.75G>C
|
|
|
ENST00000503124.5:c.1317G>C
|
ENSP00000421027.1:p.Glu439Asp
|
|
ENST00000505649.5:n.1314G>C
|
|
|
ENST00000508932.5:n.175+166G>C
|
|
|
ENST00000509063.5:c.1767G>C
|
ENSP00000422784.1:p.Glu589Asp
|
|
ENST00000511370.1:c.1300G>C
|
|
|
ENST00000621085.4:c.1128G>C
|
ENSP00000483421.1:p.Glu376Asp
|
|
ENST00000621628.4:c.1128G>C
|
ENSP00000480485.1:p.Glu376Asp
|
|
NM_000477.5:c.1767G>C
|
NP_000468.1:p.Glu589Asp
|
|
NM_000477.6:c.1767G>C
|
NP_000468.1:p.Glu589Asp
|
|
NM_000477.7:c.1767G>C
MANE Select
|
NP_000468.1:p.Glu589Asp
|
|