ENST00000355943.8:c.744A>C
MANE Select
|
ENSP00000348211.3:p.Ile248=
|
|
ENST00000355943.7:c.744A>C
|
ENSP00000348211.3:p.Ile248=
|
|
ENST00000447245.6:c.679-178A>C
|
ENSP00000399717.2:n.679-178A>C
|
|
ENST00000502462.6:n.1060A>C
|
|
|
ENST00000504098.1:c.306A>C
|
ENSP00000425708.1:p.Ile102=
|
|
ENST00000509432.1:c.105A>C
|
ENSP00000426604.1:p.Ile35=
|
|
ENST00000513706.2:n.2344A>C
|
|
|
ENST00000513807.5:c.258A>C
|
ENSP00000421134.1:p.Ile86=
|
|
NM_001303249.1:c.679-178A>C
|
NP_001290178.1:n.679-178A>C
|
|
NM_001303250.1:c.471A>C
|
NP_001290179.1:p.Ile157=
|
|
NM_138773.2:c.744A>C
|
NP_620128.1:p.Ile248=
|
|
NM_001303249.2:c.679-178A>C
|
NP_001290178.1:n.679-178A>C
|
|
NM_001303250.2:c.471A>C
|
NP_001290179.1:p.Ile157=
|
|
NM_138773.3:c.744A>C
|
NP_620128.1:p.Ile248=
|
|
NR_138151.1:n.1018A>C
|
|
|
NM_138773.4:c.744A>C
MANE Select
|
NP_620128.1:p.Ile248=
|
|
NM_001303249.3:c.679-178A>C
|
NP_001290178.1:n.679-178A>C
|
|
NM_001303250.3:c.471A>C
|
NP_001290179.1:p.Ile157=
|
|
NR_138151.2:n.983A>C
|
|
|