ENST00000322344.8:c.1406C>T
MANE Select
|
ENSP00000323511.2:p.Ser469Phe
|
|
ENST00000636840.1:c.59+117C>T
|
|
|
ENST00000640501.1:c.12C>T
|
|
|
ENST00000322344.7:c.1406C>T
|
ENSP00000323511.2:p.Ser469Phe
|
|
ENST00000593946.5:c.*1333C>T
|
ENSP00000468896.1:n.*1333C>T
|
|
ENST00000594661.5:n.1907C>T
|
|
|
ENST00000595081.5:n.309C>T
|
|
|
ENST00000596014.5:c.1406C>T
|
ENSP00000472300.1:p.Ser469Phe
|
|
ENST00000597965.2:c.113C>T
|
ENSP00000471097.2:p.Ser38Phe
|
|
ENST00000599454.5:n.326C>T
|
|
|
ENST00000600573.5:c.1313C>T
|
ENSP00000469826.1:p.Ser438Phe
|
|
ENST00000600910.5:c.1296C>T
|
ENSP00000473137.1:p.Leu432=
|
|
ENST00000601816.3:n.478C>T
|
|
|
ENST00000625216.2:c.487C>T
|
ENSP00000486898.1:n.487C>T
|
|
ENST00000627232.2:c.1326C>T
|
ENSP00000486037.1:n.1326C>T
|
|
ENST00000631020.2:c.1298C>T
|
ENSP00000486707.1:p.Ser433Phe
|
|
NM_007254.3:c.1406C>T
|
NP_009185.2:p.Ser469Phe
|
|
NM_007254.4:c.1406C>T
MANE Select
|
NP_009185.2:p.Ser469Phe
|
|