ENST00000697124.1:n.1278C>T
|
|
|
ENST00000219596.6:c.2157C>T
MANE Select
|
ENSP00000219596.1:p.Gly719=
|
|
ENST00000219596.5:c.2157C>T
|
ENSP00000219596.1:p.Gly719=
|
|
ENST00000339854.8:c.1617C>T
|
ENSP00000339639.4:p.Gly539=
|
|
ENST00000536379.5:c.1524C>T
|
ENSP00000445079.1:p.Gly508=
|
|
ENST00000536980.5:c.*433C>T
|
ENSP00000444178.1:n.*433C>T
|
|
ENST00000537682.5:c.*433C>T
|
ENSP00000438611.1:n.*433C>T
|
|
ENST00000538326.5:c.*782C>T
|
ENSP00000437486.1:n.*782C>T
|
|
ENST00000539145.5:c.1078C>T
|
ENSP00000444471.1:n.1078C>T
|
|
ENST00000541159.5:c.1699C>T
|
ENSP00000438711.1:n.1699C>T
|
|
ENST00000542898.5:c.*433C>T
|
ENSP00000444615.1:n.*433C>T
|
|
ENST00000570511.5:c.1562C>T
|
ENSP00000458312.1:n.1562C>T
|
|
ENST00000572244.5:c.847C>T
|
ENSP00000461186.1:n.847C>T
|
|
ENST00000574583.5:c.929C>T
|
ENSP00000460269.1:n.929C>T
|
|
ENST00000576315.5:c.962C>T
|
ENSP00000460551.1:n.962C>T
|
|
ENST00000621655.1:c.1694C>T
|
ENSP00000481436.1:n.1694C>T
|
|
NM_000243.2:c.2157C>T , LRG_190t1:c.2157C>T
|
NP_000234.1:p.Gly719=
|
|
NM_001198536.1:c.*361C>T
|
NP_001185465.1:n.*361C>T
|
|
XM_017023236.2:c.2154C>T
|
XP_016878725.1:p.Gly718=
|
|
NM_000243.3:c.2157C>T
MANE Select
|
NP_000234.1:p.Gly719=
|
|
NM_001198536.2:c.*361C>T
|
NP_001185465.2:n.*361C>T
|
|