ENST00000697124.1:n.912T>A
|
|
|
ENST00000219596.6:c.1791T>A
MANE Select
|
ENSP00000219596.1:p.Ala597=
|
|
ENST00000219596.5:c.1791T>A
|
ENSP00000219596.1:p.Ala597=
|
|
ENST00000339854.8:c.1251T>A
|
ENSP00000339639.4:p.Ala417=
|
|
ENST00000536379.5:c.1158T>A
|
ENSP00000445079.1:p.Ala386=
|
|
ENST00000536980.5:c.*67T>A
|
ENSP00000444178.1:n.*67T>A
|
|
ENST00000537682.5:c.*67T>A
|
ENSP00000438611.1:n.*67T>A
|
|
ENST00000538326.5:c.*416T>A
|
ENSP00000437486.1:n.*416T>A
|
|
ENST00000539145.5:c.712T>A
|
ENSP00000444471.1:n.712T>A
|
|
ENST00000541159.5:c.1333T>A
|
ENSP00000438711.1:p.Cys445Ser
|
|
ENST00000542898.5:c.*67T>A
|
ENSP00000444615.1:n.*67T>A
|
|
ENST00000570511.5:c.1196T>A
|
ENSP00000458312.1:n.1196T>A
|
|
ENST00000572244.5:c.481T>A
|
ENSP00000461186.1:n.481T>A
|
|
ENST00000574583.5:c.563T>A
|
ENSP00000460269.1:n.563T>A
|
|
ENST00000576315.5:c.596T>A
|
ENSP00000460551.1:n.596T>A
|
|
ENST00000621655.1:c.1328T>A
|
ENSP00000481436.1:n.1328T>A
|
|
NM_000243.2:c.1791T>A , LRG_190t1:c.1791T>A
|
NP_000234.1:p.Ala597=
|
|
NM_001198536.1:c.1333T>A
|
NP_001185465.1:p.Cys445Ser
|
|
XM_017023236.2:c.1788T>A
|
XP_016878725.1:p.Ala596=
|
|
XR_001751903.1:n.2098T>A
|
|
|
NM_000243.3:c.1791T>A
MANE Select
|
NP_000234.1:p.Ala597=
|
|
NM_001198536.2:c.1333T>A
|
NP_001185465.2:p.Cys445Ser
|
|