ENST00000220616.9:c.8163C>G
MANE Select
|
ENSP00000220616.4:p.Tyr2721Ter
|
|
ENST00000220616.8:c.8163C>G
|
ENSP00000220616.4:p.Tyr2721Ter
|
|
ENST00000519178.5:c.3529C>G
|
|
|
ENST00000519543.5:c.2562C>G
|
ENSP00000430430.1:p.Tyr854Ter
|
|
ENST00000521107.1:c.375C>G
|
ENSP00000430161.1:p.Tyr125Ter
|
|
ENST00000522691.1:n.249C>G
|
|
|
ENST00000523756.5:c.4818C>G
|
|
|
NM_003235.4:c.8163C>G
|
NP_003226.4:p.Tyr2721Ter
|
|
XM_005251038.3:c.7971C>G
|
XP_005251095.1:p.Tyr2657Ter
|
|
XM_006716622.2:c.8100C>G
|
XP_006716685.1:p.Tyr2700Ter
|
|
XM_005251038.4:c.7971C>G
|
XP_005251095.1:p.Tyr2657Ter
|
|
XM_006716622.3:c.8100C>G
|
XP_006716685.1:p.Tyr2700Ter
|
|
XM_017013793.1:c.8097C>G
|
XP_016869282.1:p.Tyr2699Ter
|
|
XM_017013794.1:c.8028C>G
|
XP_016869283.1:p.Tyr2676Ter
|
|
XM_017013795.1:c.7992C>G
|
XP_016869284.1:p.Tyr2664Ter
|
|
XM_017013796.1:c.7944C>G
|
XP_016869285.1:p.Tyr2648Ter
|
|
XM_017013797.1:c.7902C>G
|
XP_016869286.1:p.Tyr2634Ter
|
|
NM_003235.5:c.8163C>G
MANE Select
|
NP_003226.4:p.Tyr2721Ter
|
|