ENST00000610179.7:c.1047G>C
MANE Select
|
ENSP00000477429.2:p.Glu349Asp
|
|
ENST00000316562.9:c.1377G>C
|
ENSP00000313377.4:p.Glu459Asp
|
|
ENST00000336066.8:c.*388G>C
|
ENSP00000477229.2:n.*388G>C
|
|
ENST00000610179.6:c.1047G>C
|
ENSP00000477429.2:p.Glu349Asp
|
|
ENST00000643504.2:c.*677G>C
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ENSP00000495157.2:n.*677G>C
|
|
ENST00000646394.1:c.874G>C
|
|
|
ENST00000316562.8:c.1377G>C
|
ENSP00000313377.4:p.Glu459Asp
|
|
ENST00000336066.7:c.*388G>C
|
ENSP00000477229.1:n.*388G>C
|
|
ENST00000464452.1:n.612G>C
|
|
|
ENST00000495692.5:c.69G>C
|
ENSP00000476745.1:p.Glu23Asp
|
|
ENST00000497424.5:c.504G>C
|
ENSP00000417609.1:p.Glu168Asp
|
|
ENST00000610179.5:c.1008G>C
|
ENSP00000477429.1:p.Glu336Asp
|
|
ENST00000621507.1:c.504G>C
|
ENSP00000481523.1:p.Glu168Asp
|
|
NM_024960.4:c.504G>C
|
NP_079236.3:p.Glu168Asp
|
|
NM_153638.2:c.1377G>C
|
NP_705902.2:p.Glu459Asp
|
|
NM_153640.2:c.504G>C
|
NP_705904.1:p.Glu168Asp
|
|
XM_005260835.2:c.762G>C
|
XP_005260892.1:p.Glu254Asp
|
|
XM_005260836.3:c.504G>C
|
XP_005260893.3:p.Glu168Asp
|
|
XM_006723631.1:c.504G>C
|
XP_006723694.1:p.Glu168Asp
|
|
XM_011529364.1:c.1235+1769G>C
|
XP_011527666.1:n.1235+1769G>C
|
|
NM_001324191.1:c.504G>C
|
NP_001311120.1:p.Glu168Asp
|
|
NM_001324193.1:c.69G>C
|
NP_001311122.1:p.Glu23Asp
|
|
NM_024960.5:c.504G>C
|
NP_079236.3:p.Glu168Asp
|
|
NM_153638.3:c.1377G>C
|
NP_705902.2:p.Glu459Asp
|
|
NM_153640.3:c.504G>C
|
NP_705904.1:p.Glu168Asp
|
|
NR_136715.1:n.1401G>C
|
|
|
XM_005260835.3:c.762G>C
|
XP_005260892.1:p.Glu254Asp
|
|
XM_005260836.4:c.504G>C
|
XP_005260893.3:p.Glu168Asp
|
|
XM_011529364.3:c.1235+1769G>C
|
XP_011527666.1:n.1235+1769G>C
|
|
XM_017028077.2:c.69G>C
|
XP_016883566.1:p.Glu23Asp
|
|
XM_017028078.2:c.69G>C
|
XP_016883567.1:p.Glu23Asp
|
|
XM_017028079.2:c.69G>C
|
XP_016883568.1:p.Glu23Asp
|
|
XM_024452002.1:c.69G>C
|
XP_024307770.1:p.Glu23Asp
|
|
XR_002958533.1:n.2165G>C
|
|
|
NM_001324191.2:c.504G>C
|
NP_001311120.1:p.Glu168Asp
|
|
NM_001324193.2:c.69G>C
|
NP_001311122.1:p.Glu23Asp
|
|
NM_024960.6:c.504G>C
|
NP_079236.3:p.Glu168Asp
|
|
NR_136715.2:n.948G>C
|
|
|
NM_001386393.1:c.1047G>C
MANE Select
|
NP_001373322.1:p.Glu349Asp
|
|
NM_153638.4:c.1377G>C
|
NP_705902.2:p.Glu459Asp
|
|
NM_153640.4:c.504G>C
|
NP_705904.1:p.Glu168Asp
|
|