ENST00000478003.2:n.1871C>G
|
|
|
ENST00000682276.1:n.1488C>G
|
|
|
ENST00000682892.1:c.1590C>G
|
ENSP00000507214.1:p.Asp530Glu
|
|
ENST00000682952.1:n.1682C>G
|
|
|
ENST00000684455.1:c.1256C>G
|
|
|
ENST00000684642.1:c.1440C>G
|
ENSP00000507355.1:p.Asp480Glu
|
|
ENST00000684740.1:n.2221C>G
|
|
|
ENST00000303236.9:c.2043C>G
MANE Select
|
ENSP00000307235.3:p.Asp681Glu
|
|
ENST00000652099.1:c.2237C>G
|
|
|
ENST00000652736.1:n.1919C>G
|
|
|
ENST00000303236.7:c.2043C>G
|
ENSP00000307235.3:p.Asp681Glu
|
|
ENST00000415570.1:c.1680C>G
|
ENSP00000412076.1:p.Asp560Glu
|
|
ENST00000419748.5:c.1590C>G
|
ENSP00000408325.1:p.Asp530Glu
|
|
ENST00000478003.1:n.609C>G
|
|
|
NM_001313915.1:c.1590C>G
|
NP_001300844.1:p.Asp530Glu
|
|
NM_004836.5:c.2043C>G
|
NP_004827.4:p.Asp681Glu
|
|
NM_004836.6:c.2043C>G
|
NP_004827.4:p.Asp681Glu
|
|
NR_110236.1:n.1577G>C
|
|
|
XM_005264649.3:c.1359C>G
|
XP_005264706.1:p.Asp453Glu
|
|
XR_939749.1:n.2322C>G
|
|
|
XM_017005376.2:c.1359C>G
|
XP_016860865.1:p.Asp453Glu
|
|
NM_004836.7:c.2043C>G
MANE Select
|
NP_004827.4:p.Asp681Glu
|
|
NM_001313915.2:c.1590C>G
|
NP_001300844.1:p.Asp530Glu
|
|