ENST00000369458.8:c.849A>G
MANE Select
|
ENSP00000358470.3:p.Ter283=
|
|
ENST00000328189.7:c.501A>G
|
ENSP00000328168.3:p.Ter167=
|
|
ENST00000359008.8:c.858A>G
|
ENSP00000351899.4:p.Ter286=
|
|
ENST00000369458.7:c.849A>G
|
ENSP00000358470.3:p.Ter283=
|
|
ENST00000539893.5:c.564A>G
|
ENSP00000444724.1:p.Ter188=
|
|
NM_001253849.1:c.564A>G
|
NP_001240778.1:p.Ter188=
|
|
NM_001253850.1:c.501A>G
|
NP_001240779.1:p.Ter167=
|
|
NM_024626.3:c.849A>G
|
NP_078902.2:p.Ter283=
|
|
NR_045603.1:n.1044A>G
|
|
|
NR_045604.1:n.748A>G
|
|
|
XM_011542143.1:c.900A>G
|
XP_011540445.1:p.Ter300=
|
|
XM_011542144.1:c.903A>G
|
XP_011540446.1:p.Ter301=
|
|
XM_011542145.1:c.864A>G
|
XP_011540447.1:p.Ter288=
|
|
XM_011542143.2:c.999A>G
|
XP_011540445.2:p.Ter333=
|
|
XM_017002335.2:c.864A>G
|
XP_016857824.1:p.Ter288=
|
|
NM_024626.4:c.849A>G
MANE Select
|
NP_078902.2:p.Ter283=
|
|
NR_045603.2:n.1011A>G
|
|
|
NR_045604.2:n.715A>G
|
|
|
NM_001253849.2:c.564A>G
|
NP_001240778.1:p.Ter188=
|
|
NM_001253850.2:c.501A>G
|
NP_001240779.1:p.Ter167=
|
|