ENST00000220616.9:c.8157C>G
MANE Select
|
ENSP00000220616.4:p.Ser2719=
|
|
ENST00000220616.8:c.8157C>G
|
ENSP00000220616.4:p.Ser2719=
|
|
ENST00000519178.5:c.3523C>G
|
|
|
ENST00000519543.5:c.2556C>G
|
ENSP00000430430.1:p.Ser852=
|
|
ENST00000521107.1:c.369C>G
|
ENSP00000430161.1:p.Ser123=
|
|
ENST00000522691.1:n.243C>G
|
|
|
ENST00000523756.5:c.4812C>G
|
|
|
NM_003235.4:c.8157C>G
|
NP_003226.4:p.Ser2719=
|
|
XM_005251038.3:c.7965C>G
|
XP_005251095.1:p.Ser2655=
|
|
XM_006716622.2:c.8094C>G
|
XP_006716685.1:p.Ser2698=
|
|
XM_005251038.4:c.7965C>G
|
XP_005251095.1:p.Ser2655=
|
|
XM_006716622.3:c.8094C>G
|
XP_006716685.1:p.Ser2698=
|
|
XM_017013793.1:c.8091C>G
|
XP_016869282.1:p.Ser2697=
|
|
XM_017013794.1:c.8022C>G
|
XP_016869283.1:p.Ser2674=
|
|
XM_017013795.1:c.7986C>G
|
XP_016869284.1:p.Ser2662=
|
|
XM_017013796.1:c.7938C>G
|
XP_016869285.1:p.Ser2646=
|
|
XM_017013797.1:c.7896C>G
|
XP_016869286.1:p.Ser2632=
|
|
NM_003235.5:c.8157C>G
MANE Select
|
NP_003226.4:p.Ser2719=
|
|