|
ENST00000355943.8:c.389A=
MANE Select
|
ENSP00000348211.3:p.Asn130=
|
|
|
ENST00000355943.7:c.389A=
|
ENSP00000348211.3:p.Asn130=
|
|
|
ENST00000447245.6:c.389A=
|
ENSP00000399717.2:p.Asn130=
|
|
|
ENST00000502462.6:n.705A=
|
|
|
|
ENST00000504098.1:c.-50A=
|
ENSP00000425708.1:n.-50A=
|
|
|
ENST00000508781.5:n.218A=
|
|
|
|
ENST00000513807.5:c.-98A=
|
ENSP00000421134.1:n.-98A=
|
|
|
NM_001303249.1:c.389A=
|
NP_001290178.1:p.Asn130=
|
|
|
NM_001303250.1:c.116A=
|
NP_001290179.1:p.Asn39=
|
|
|
NM_138773.2:c.389A=
|
NP_620128.1:p.Asn130=
|
|
|
XM_011543708.1:c.389A=
|
XP_011542010.1:p.Asn130=
|
|
|
NM_001303249.2:c.389A=
|
NP_001290178.1:p.Asn130=
|
|
|
NM_001303250.2:c.116A=
|
NP_001290179.1:p.Asn39=
|
|
|
NM_138773.3:c.389A=
|
NP_620128.1:p.Asn130=
|
|
|
NR_138151.1:n.537A=
|
|
|
|
NM_138773.4:c.389A=
MANE Select
|
NP_620128.1:p.Asn130=
|
|
|
NM_001303249.3:c.389A=
|
NP_001290178.1:p.Asn130=
|
|
|
NM_001303250.3:c.116A=
|
NP_001290179.1:p.Asn39=
|
|
|
NR_138151.2:n.502A=
|
|
|
