ENST00000309383.6:c.2145C>G
MANE Select
|
ENSP00000310649.1:p.Ser715Arg
|
|
ENST00000309383.5:c.2145C>G
|
ENSP00000310649.1:p.Ser715Arg
|
|
ENST00000326848.7:c.1230C>G
|
ENSP00000320853.7:p.Ser410Arg
|
|
ENST00000590333.5:c.2193C>G
|
ENSP00000468190.1:p.Ser731Arg
|
|
NM_032430.1:c.2145C>G
|
NP_115806.1:p.Ser715Arg
|
|
XM_005259327.2:c.1875C>G
|
XP_005259384.1:p.Ser625Arg
|
|
XM_011527395.1:c.1902C>G
|
XP_011525697.1:p.Ser634Arg
|
|
XR_430213.2:n.2128C>G
|
|
|
XM_005259327.3:c.1875C>G
|
XP_005259384.1:p.Ser625Arg
|
|
XM_011527395.2:c.1617C>G
|
XP_011525697.2:p.Ser539Arg
|
|
XM_024451739.1:c.1920C>G
|
XP_024307507.1:p.Ser640Arg
|
|
XR_430213.4:n.2426C>G
|
|
|
NM_032430.2:c.2145C>G
MANE Select
|
NP_115806.1:p.Ser715Arg
|
|