ENST00000355943.8:c.1192C>T
MANE Select
|
ENSP00000348211.3:p.Leu398=
|
|
ENST00000355943.7:c.1192C>T
|
ENSP00000348211.3:p.Leu398=
|
|
ENST00000447245.6:c.949C>T
|
ENSP00000399717.2:p.Leu317=
|
|
ENST00000504098.1:c.754C>T
|
ENSP00000425708.1:p.Leu252=
|
|
ENST00000509432.1:c.553C>T
|
ENSP00000426604.1:p.Leu185=
|
|
ENST00000513706.2:n.2792C>T
|
|
|
ENST00000513807.5:c.706C>T
|
ENSP00000421134.1:p.Leu236=
|
|
NM_001303249.1:c.949C>T
|
NP_001290178.1:p.Leu317=
|
|
NM_001303250.1:c.919C>T
|
NP_001290179.1:p.Leu307=
|
|
NM_138773.2:c.1192C>T
|
NP_620128.1:p.Leu398=
|
|
NM_001303249.2:c.949C>T
|
NP_001290178.1:p.Leu317=
|
|
NM_001303250.2:c.919C>T
|
NP_001290179.1:p.Leu307=
|
|
NM_138773.3:c.1192C>T
|
NP_620128.1:p.Leu398=
|
|
NR_138151.1:n.1466C>T
|
|
|
NM_138773.4:c.1192C>T
MANE Select
|
NP_620128.1:p.Leu398=
|
|
NM_001303249.3:c.949C>T
|
NP_001290178.1:p.Leu317=
|
|
NM_001303250.3:c.919C>T
|
NP_001290179.1:p.Leu307=
|
|
NR_138151.2:n.1431C>T
|
|
|