ENST00000404085.7:c.567A>C
MANE Select
|
ENSP00000384008.3:p.Gly189=
|
|
ENST00000404261.9:c.567A>C
|
ENSP00000384753.6:p.Gly189=
|
|
ENST00000594072.6:c.567A>C
|
ENSP00000468845.4:p.Gly189=
|
|
ENST00000651416.1:n.784A>C
|
|
|
ENST00000652132.1:c.534A>C
|
ENSP00000498416.1:p.Gly178=
|
|
ENST00000394458.7:c.729A>C
|
ENSP00000377971.4:p.Gly243=
|
|
ENST00000404085.5:c.*466A>C
|
ENSP00000384008.2:n.*466A>C
|
|
ENST00000404261.8:c.729A>C
|
ENSP00000384753.5:p.Gly243=
|
|
ENST00000594072.5:c.729A>C
|
ENSP00000468845.3:p.Gly243=
|
|
ENST00000596626.1:n.680A>C
|
|
|
ENST00000598347.2:c.569A>C
|
|
|
NM_001278443.1:c.696A>C
|
NP_001265372.1:p.Gly232=
|
|
NM_001278444.1:c.729A>C
|
NP_001265373.1:p.Gly243=
|
|
NM_001278445.1:c.633A>C
|
NP_001265374.1:p.Gly211=
|
|
NM_152363.5:c.729A>C
|
NP_689576.5:p.Gly243=
|
|
NR_103530.1:n.843A>C
|
|
|
NM_001278443.2:c.534A>C
|
NP_001265372.2:p.Gly178=
|
|
NM_001278444.2:c.567A>C
|
NP_001265373.2:p.Gly189=
|
|
NM_001278445.2:c.525A>C
|
NP_001265374.2:p.Gly175=
|
|
NM_152363.6:c.567A>C
MANE Select
|
NP_689576.6:p.Gly189=
|
|
NR_103530.2:n.587A>C
|
|
|