ENST00000695558.1:c.5634A>C
|
ENSP00000512015.1:p.Glu1878Asp
|
|
ENST00000703224.1:c.*4844A>C
|
ENSP00000515242.1:n.*4844A>C
|
|
ENST00000359568.10:c.5601A>C
MANE Select
|
ENSP00000352572.5:p.Glu1867Asp
|
|
ENST00000359568.9:c.5601A>C
|
ENSP00000352572.5:p.Glu1867Asp
|
|
ENST00000480896.5:n.5870A>C
|
|
|
NM_001315529.1:c.5247A>C
|
NP_001302458.1:p.Glu1749Asp
|
|
NM_006031.5:c.5601A>C
|
NP_006022.3:p.Glu1867Asp
|
|
XM_005261124.3:c.5634A>C
|
XP_005261181.1:p.Glu1878Asp
|
|
XM_011529593.1:c.5712A>C
|
XP_011527895.1:p.Glu1904Asp
|
|
XM_011529594.1:c.5682A>C
|
XP_011527896.1:p.Glu1894Asp
|
|
XM_005261124.5:c.5634A>C
|
XP_005261181.1:p.Glu1878Asp
|
|
XM_011529594.3:c.5682A>C
|
XP_011527896.1:p.Glu1894Asp
|
|
XM_017028362.2:c.5601A>C
|
XP_016883851.1:p.Glu1867Asp
|
|
XM_017028363.1:c.5280A>C
|
XP_016883852.1:p.Glu1760Asp
|
|
XM_024452082.1:c.4518A>C
|
XP_024307850.1:p.Glu1506Asp
|
|
XM_024452083.1:c.3414A>C
|
XP_024307851.1:p.Glu1138Asp
|
|
NM_006031.6:c.5601A>C
MANE Select
|
NP_006022.3:p.Glu1867Asp
|
|
NM_001315529.2:c.5247A>C
|
NP_001302458.1:p.Glu1749Asp
|
|