ENST00000322344.8:c.1443C>A
MANE Select
|
ENSP00000323511.2:p.Gly481=
|
|
ENST00000636840.1:c.59+154C>A
|
|
|
ENST00000640501.1:c.49C>A
|
|
|
ENST00000322344.7:c.1443C>A
|
ENSP00000323511.2:p.Gly481=
|
|
ENST00000593946.5:c.*1370C>A
|
ENSP00000468896.1:n.*1370C>A
|
|
ENST00000594661.5:n.1944C>A
|
|
|
ENST00000595081.5:n.346C>A
|
|
|
ENST00000596014.5:c.1443C>A
|
ENSP00000472300.1:p.Gly481=
|
|
ENST00000597965.2:c.150C>A
|
ENSP00000471097.2:p.Gly50=
|
|
ENST00000599454.5:n.363C>A
|
|
|
ENST00000600573.5:c.1350C>A
|
ENSP00000469826.1:p.Gly450=
|
|
ENST00000600910.5:c.1333C>A
|
ENSP00000473137.1:p.Leu445Ile
|
|
ENST00000601816.3:n.515C>A
|
|
|
ENST00000625216.2:c.524C>A
|
ENSP00000486898.1:n.524C>A
|
|
ENST00000627232.2:c.1363C>A
|
ENSP00000486037.1:n.1363C>A
|
|
ENST00000631020.2:c.1335C>A
|
ENSP00000486707.1:p.Gly445=
|
|
NM_007254.3:c.1443C>A
|
NP_009185.2:p.Gly481=
|
|
NM_007254.4:c.1443C>A
MANE Select
|
NP_009185.2:p.Gly481=
|
|