ENST00000355943.8:c.726A>C
MANE Select
|
ENSP00000348211.3:p.Glu242Asp
|
|
ENST00000355943.7:c.726A>C
|
ENSP00000348211.3:p.Glu242Asp
|
|
ENST00000447245.6:c.679-196A>C
|
ENSP00000399717.2:n.679-196A>C
|
|
ENST00000502462.6:n.1042A>C
|
|
|
ENST00000504098.1:c.288A>C
|
ENSP00000425708.1:p.Glu96Asp
|
|
ENST00000509432.1:c.87A>C
|
ENSP00000426604.1:p.Glu29Asp
|
|
ENST00000513706.2:n.2326A>C
|
|
|
ENST00000513807.5:c.240A>C
|
ENSP00000421134.1:p.Glu80Asp
|
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NM_001303249.1:c.679-196A>C
|
NP_001290178.1:n.679-196A>C
|
|
NM_001303250.1:c.453A>C
|
NP_001290179.1:p.Glu151Asp
|
|
NM_138773.2:c.726A>C
|
NP_620128.1:p.Glu242Asp
|
|
NM_001303249.2:c.679-196A>C
|
NP_001290178.1:n.679-196A>C
|
|
NM_001303250.2:c.453A>C
|
NP_001290179.1:p.Glu151Asp
|
|
NM_138773.3:c.726A>C
|
NP_620128.1:p.Glu242Asp
|
|
NR_138151.1:n.1000A>C
|
|
|
NM_138773.4:c.726A>C
MANE Select
|
NP_620128.1:p.Glu242Asp
|
|
NM_001303249.3:c.679-196A>C
|
NP_001290178.1:n.679-196A>C
|
|
NM_001303250.3:c.453A>C
|
NP_001290179.1:p.Glu151Asp
|
|
NR_138151.2:n.965A>C
|
|
|