ENST00000220616.9:c.8091C>G
MANE Select
|
ENSP00000220616.4:p.Tyr2697Ter
|
|
ENST00000220616.8:c.8091C>G
|
ENSP00000220616.4:p.Tyr2697Ter
|
|
ENST00000519178.5:c.3457C>G
|
|
|
ENST00000519543.5:c.2490C>G
|
ENSP00000430430.1:p.Tyr830Ter
|
|
ENST00000521107.1:c.303C>G
|
ENSP00000430161.1:p.Tyr101Ter
|
|
ENST00000522691.1:n.177C>G
|
|
|
ENST00000523756.5:c.4746C>G
|
|
|
NM_003235.4:c.8091C>G
|
NP_003226.4:p.Tyr2697Ter
|
|
XM_005251038.3:c.7899C>G
|
XP_005251095.1:p.Tyr2633Ter
|
|
XM_006716622.2:c.8028C>G
|
XP_006716685.1:p.Tyr2676Ter
|
|
XM_005251038.4:c.7899C>G
|
XP_005251095.1:p.Tyr2633Ter
|
|
XM_006716622.3:c.8028C>G
|
XP_006716685.1:p.Tyr2676Ter
|
|
XM_017013793.1:c.8025C>G
|
XP_016869282.1:p.Tyr2675Ter
|
|
XM_017013794.1:c.7956C>G
|
XP_016869283.1:p.Tyr2652Ter
|
|
XM_017013795.1:c.7920C>G
|
XP_016869284.1:p.Tyr2640Ter
|
|
XM_017013796.1:c.7872C>G
|
XP_016869285.1:p.Tyr2624Ter
|
|
XM_017013797.1:c.7830C>G
|
XP_016869286.1:p.Tyr2610Ter
|
|
NM_003235.5:c.8091C>G
MANE Select
|
NP_003226.4:p.Tyr2697Ter
|
|