ENST00000322344.8:c.1387T>A
MANE Select
|
ENSP00000323511.2:p.Phe463Ile
|
|
ENST00000636840.1:c.59+98T>A
|
|
|
ENST00000322344.7:c.1387T>A
|
ENSP00000323511.2:p.Phe463Ile
|
|
ENST00000593946.5:c.*1314T>A
|
ENSP00000468896.1:n.*1314T>A
|
|
ENST00000594661.5:n.1888T>A
|
|
|
ENST00000595081.5:n.290T>A
|
|
|
ENST00000596014.5:c.1387T>A
|
ENSP00000472300.1:p.Phe463Ile
|
|
ENST00000597965.2:c.94T>A
|
ENSP00000471097.2:p.Phe32Ile
|
|
ENST00000599454.5:n.307T>A
|
|
|
ENST00000600573.5:c.1294T>A
|
ENSP00000469826.1:p.Phe432Ile
|
|
ENST00000600910.5:c.1277T>A
|
ENSP00000473137.1:p.Val426Asp
|
|
ENST00000601816.3:n.459T>A
|
|
|
ENST00000625216.2:c.468T>A
|
ENSP00000486898.1:n.468T>A
|
|
ENST00000627232.2:c.1307T>A
|
ENSP00000486037.1:n.1307T>A
|
|
ENST00000631020.2:c.1279T>A
|
ENSP00000486707.1:p.Phe427Ile
|
|
NM_007254.3:c.1387T>A
|
NP_009185.2:p.Phe463Ile
|
|
NM_007254.4:c.1387T>A
MANE Select
|
NP_009185.2:p.Phe463Ile
|
|