ENST00000322344.8:c.1407C>G
MANE Select
|
ENSP00000323511.2:p.Ser469=
|
|
ENST00000636840.1:c.59+118C>G
|
|
|
ENST00000640501.1:c.13C>G
|
|
|
ENST00000322344.7:c.1407C>G
|
ENSP00000323511.2:p.Ser469=
|
|
ENST00000593946.5:c.*1334C>G
|
ENSP00000468896.1:n.*1334C>G
|
|
ENST00000594661.5:n.1908C>G
|
|
|
ENST00000595081.5:n.310C>G
|
|
|
ENST00000596014.5:c.1407C>G
|
ENSP00000472300.1:p.Ser469=
|
|
ENST00000597965.2:c.114C>G
|
ENSP00000471097.2:p.Ser38=
|
|
ENST00000599454.5:n.327C>G
|
|
|
ENST00000600573.5:c.1314C>G
|
ENSP00000469826.1:p.Ser438=
|
|
ENST00000600910.5:c.1297C>G
|
ENSP00000473137.1:p.Leu433Val
|
|
ENST00000601816.3:n.479C>G
|
|
|
ENST00000625216.2:c.488C>G
|
ENSP00000486898.1:n.488C>G
|
|
ENST00000627232.2:c.1327C>G
|
ENSP00000486037.1:n.1327C>G
|
|
ENST00000631020.2:c.1299C>G
|
ENSP00000486707.1:p.Ser433=
|
|
NM_007254.3:c.1407C>G
|
NP_009185.2:p.Ser469=
|
|
NM_007254.4:c.1407C>G
MANE Select
|
NP_009185.2:p.Ser469=
|
|