ENST00000328300.11:c.5057T>C
MANE Select
|
ENSP00000331902.7:p.Val1686Ala
|
|
ENST00000361603.7:c.5039T>C
|
ENSP00000354505.2:p.Val1680Ala
|
|
ENST00000510690.2:n.1551T>C
|
|
|
ENST00000644079.1:n.2745T>C
|
|
|
ENST00000328300.10:c.5057T>C
|
ENSP00000331902.6:p.Val1686Ala
|
|
ENST00000361603.6:c.5039T>C
|
ENSP00000354505.2:p.Val1680Ala
|
|
ENST00000504541.1:c.282T>C
|
ENSP00000424845.1:n.282T>C
|
|
ENST00000515658.1:c.387T>C
|
|
|
NM_000495.4:c.5039T>C
|
NP_000486.1:p.Val1680Ala
|
|
NM_033380.2:c.5057T>C
|
NP_203699.1:p.Val1686Ala
|
|
XM_005262070.2:c.5048T>C
|
XP_005262127.1:p.Val1683Ala
|
|
XM_006724616.2:c.5057T>C
|
XP_006724679.1:p.Val1686Ala
|
|
XM_011530849.1:c.4733T>C
|
XP_011529151.1:p.Val1578Ala
|
|
XM_011530851.1:c.2630T>C
|
XP_011529153.1:p.Val877Ala
|
|
XM_011530849.2:c.5072T>C
|
XP_011529151.2:p.Val1691Ala
|
|
XM_017029259.2:c.5063T>C
|
XP_016884748.1:p.Val1688Ala
|
|
XM_017029260.1:c.5054T>C
|
XP_016884749.1:p.Val1685Ala
|
|
XM_017029263.2:c.3392T>C
|
XP_016884752.1:p.Val1131Ala
|
|
NM_000495.5:c.5039T>C
|
NP_000486.1:p.Val1680Ala
|
|
NM_033380.3:c.5057T>C
MANE Select
|
NP_203699.1:p.Val1686Ala
|
|