ENST00000309383.6:c.2161T>G
MANE Select
|
ENSP00000310649.1:p.Ser721Ala
|
|
ENST00000309383.5:c.2161T>G
|
ENSP00000310649.1:p.Ser721Ala
|
|
ENST00000326848.7:c.1246T>G
|
ENSP00000320853.7:p.Ser416Ala
|
|
ENST00000590333.5:c.2209T>G
|
ENSP00000468190.1:p.Ser737Ala
|
|
NM_032430.1:c.2161T>G
|
NP_115806.1:p.Ser721Ala
|
|
XM_005259327.2:c.1891T>G
|
XP_005259384.1:p.Ser631Ala
|
|
XM_011527395.1:c.1918T>G
|
XP_011525697.1:p.Ser640Ala
|
|
XR_430213.2:n.2144T>G
|
|
|
XM_005259327.3:c.1891T>G
|
XP_005259384.1:p.Ser631Ala
|
|
XM_011527395.2:c.1633T>G
|
XP_011525697.2:p.Ser545Ala
|
|
XM_024451739.1:c.1936T>G
|
XP_024307507.1:p.Ser646Ala
|
|
XR_430213.4:n.2442T>G
|
|
|
NM_032430.2:c.2161T>G
MANE Select
|
NP_115806.1:p.Ser721Ala
|
|