ENST00000355943.8:c.1230C>T
MANE Select
|
ENSP00000348211.3:p.Tyr410=
|
|
ENST00000355943.7:c.1230C>T
|
ENSP00000348211.3:p.Tyr410=
|
|
ENST00000447245.6:c.987C>T
|
ENSP00000399717.2:p.Tyr329=
|
|
ENST00000504098.1:c.792C>T
|
ENSP00000425708.1:p.Tyr264=
|
|
ENST00000509432.1:c.591C>T
|
ENSP00000426604.1:p.Tyr197=
|
|
ENST00000513706.2:n.2830C>T
|
|
|
ENST00000513807.5:c.744C>T
|
ENSP00000421134.1:p.Tyr248=
|
|
NM_001303249.1:c.987C>T
|
NP_001290178.1:p.Tyr329=
|
|
NM_001303250.1:c.957C>T
|
NP_001290179.1:p.Tyr319=
|
|
NM_138773.2:c.1230C>T
|
NP_620128.1:p.Tyr410=
|
|
NM_001303249.2:c.987C>T
|
NP_001290178.1:p.Tyr329=
|
|
NM_001303250.2:c.957C>T
|
NP_001290179.1:p.Tyr319=
|
|
NM_138773.3:c.1230C>T
|
NP_620128.1:p.Tyr410=
|
|
NR_138151.1:n.1504C>T
|
|
|
NM_138773.4:c.1230C>T
MANE Select
|
NP_620128.1:p.Tyr410=
|
|
NM_001303249.3:c.987C>T
|
NP_001290178.1:p.Tyr329=
|
|
NM_001303250.3:c.957C>T
|
NP_001290179.1:p.Tyr319=
|
|
NR_138151.2:n.1469C>T
|
|
|