ENST00000309383.6:c.2162C>A
MANE Select
|
ENSP00000310649.1:p.Ser721Tyr
|
|
ENST00000309383.5:c.2162C>A
|
ENSP00000310649.1:p.Ser721Tyr
|
|
ENST00000326848.7:c.1247C>A
|
ENSP00000320853.7:p.Ser416Tyr
|
|
ENST00000590333.5:c.2210C>A
|
ENSP00000468190.1:p.Ser737Tyr
|
|
NM_032430.1:c.2162C>A
|
NP_115806.1:p.Ser721Tyr
|
|
XM_005259327.2:c.1892C>A
|
XP_005259384.1:p.Ser631Tyr
|
|
XM_011527395.1:c.1919C>A
|
XP_011525697.1:p.Ser640Tyr
|
|
XR_430213.2:n.2145C>A
|
|
|
XM_005259327.3:c.1892C>A
|
XP_005259384.1:p.Ser631Tyr
|
|
XM_011527395.2:c.1634C>A
|
XP_011525697.2:p.Ser545Tyr
|
|
XM_024451739.1:c.1937C>A
|
XP_024307507.1:p.Ser646Tyr
|
|
XR_430213.4:n.2443C>A
|
|
|
NM_032430.2:c.2162C>A
MANE Select
|
NP_115806.1:p.Ser721Tyr
|
|