ENST00000355943.8:c.693A>C
MANE Select
|
ENSP00000348211.3:p.Arg231=
|
|
ENST00000355943.7:c.693A>C
|
ENSP00000348211.3:p.Arg231=
|
|
ENST00000447245.6:c.679-229A>C
|
ENSP00000399717.2:n.679-229A>C
|
|
ENST00000502462.6:n.1009A>C
|
|
|
ENST00000504098.1:c.255A>C
|
ENSP00000425708.1:p.Arg85=
|
|
ENST00000509432.1:c.54A>C
|
ENSP00000426604.1:p.Arg18=
|
|
ENST00000513706.2:n.2293A>C
|
|
|
ENST00000513807.5:c.207A>C
|
ENSP00000421134.1:p.Arg69=
|
|
NM_001303249.1:c.679-229A>C
|
NP_001290178.1:n.679-229A>C
|
|
NM_001303250.1:c.420A>C
|
NP_001290179.1:p.Arg140=
|
|
NM_138773.2:c.693A>C
|
NP_620128.1:p.Arg231=
|
|
NM_001303249.2:c.679-229A>C
|
NP_001290178.1:n.679-229A>C
|
|
NM_001303250.2:c.420A>C
|
NP_001290179.1:p.Arg140=
|
|
NM_138773.3:c.693A>C
|
NP_620128.1:p.Arg231=
|
|
NR_138151.1:n.967A>C
|
|
|
NM_138773.4:c.693A>C
MANE Select
|
NP_620128.1:p.Arg231=
|
|
NM_001303249.3:c.679-229A>C
|
NP_001290178.1:n.679-229A>C
|
|
NM_001303250.3:c.420A>C
|
NP_001290179.1:p.Arg140=
|
|
NR_138151.2:n.932A>C
|
|
|