ENST00000649368.1:c.1304C>T
MANE Select
|
ENSP00000496793.1:p.Ala435Val
|
|
ENST00000343916.7:c.1304C>T
|
ENSP00000341640.3:p.Ala435Val
|
|
ENST00000466192.5:n.1031C>T
|
|
|
ENST00000469852.5:n.600C>T
|
|
|
ENST00000481800.1:n.277C>T
|
|
|
ENST00000490398.5:n.101C>T
|
|
|
NM_001853.3:c.1304C>T
|
NP_001844.3:p.Ala435Val
|
|
XM_011528543.1:c.1304C>T
|
XP_011526845.1:p.Ala435Val
|
|
XM_011528544.1:c.1097C>T
|
XP_011526846.1:p.Ala366Val
|
|
XM_011528545.1:c.1304C>T
|
XP_011526847.1:p.Ala435Val
|
|
XM_011528546.1:c.1304C>T
|
XP_011526848.1:p.Ala435Val
|
|
XM_011528547.1:c.1304C>T
|
XP_011526849.1:p.Ala435Val
|
|
XR_936499.1:n.1305C>T
|
|
|
NM_001853.4:c.1304C>T
MANE Select
|
NP_001844.3:p.Ala435Val
|
|
XM_017027666.1:c.1304C>T
|
XP_016883155.1:p.Ala435Val
|
|