ENST00000322344.8:c.1388T>G
MANE Select
|
ENSP00000323511.2:p.Phe463Cys
|
|
ENST00000636840.1:c.59+99T>G
|
|
|
ENST00000322344.7:c.1388T>G
|
ENSP00000323511.2:p.Phe463Cys
|
|
ENST00000593946.5:c.*1315T>G
|
ENSP00000468896.1:n.*1315T>G
|
|
ENST00000594661.5:n.1889T>G
|
|
|
ENST00000595081.5:n.291T>G
|
|
|
ENST00000596014.5:c.1388T>G
|
ENSP00000472300.1:p.Phe463Cys
|
|
ENST00000597965.2:c.95T>G
|
ENSP00000471097.2:p.Phe32Cys
|
|
ENST00000599454.5:n.308T>G
|
|
|
ENST00000600573.5:c.1295T>G
|
ENSP00000469826.1:p.Phe432Cys
|
|
ENST00000600910.5:c.1278T>G
|
ENSP00000473137.1:p.Val426=
|
|
ENST00000601816.3:n.460T>G
|
|
|
ENST00000625216.2:c.469T>G
|
ENSP00000486898.1:n.469T>G
|
|
ENST00000627232.2:c.1308T>G
|
ENSP00000486037.1:n.1308T>G
|
|
ENST00000631020.2:c.1280T>G
|
ENSP00000486707.1:p.Phe427Cys
|
|
NM_007254.3:c.1388T>G
|
NP_009185.2:p.Phe463Cys
|
|
NM_007254.4:c.1388T>G
MANE Select
|
NP_009185.2:p.Phe463Cys
|
|