ENST00000220616.9:c.8090A>G
MANE Select
|
ENSP00000220616.4:p.Tyr2697Cys
|
|
ENST00000220616.8:c.8090A>G
|
ENSP00000220616.4:p.Tyr2697Cys
|
|
ENST00000519178.5:c.3456A>G
|
|
|
ENST00000519543.5:c.2489A>G
|
ENSP00000430430.1:p.Tyr830Cys
|
|
ENST00000521107.1:c.302A>G
|
ENSP00000430161.1:p.Tyr101Cys
|
|
ENST00000522691.1:n.176A>G
|
|
|
ENST00000523756.5:c.4745A>G
|
|
|
NM_003235.4:c.8090A>G
|
NP_003226.4:p.Tyr2697Cys
|
|
XM_005251038.3:c.7898A>G
|
XP_005251095.1:p.Tyr2633Cys
|
|
XM_006716622.2:c.8027A>G
|
XP_006716685.1:p.Tyr2676Cys
|
|
XM_005251038.4:c.7898A>G
|
XP_005251095.1:p.Tyr2633Cys
|
|
XM_006716622.3:c.8027A>G
|
XP_006716685.1:p.Tyr2676Cys
|
|
XM_017013793.1:c.8024A>G
|
XP_016869282.1:p.Tyr2675Cys
|
|
XM_017013794.1:c.7955A>G
|
XP_016869283.1:p.Tyr2652Cys
|
|
XM_017013795.1:c.7919A>G
|
XP_016869284.1:p.Tyr2640Cys
|
|
XM_017013796.1:c.7871A>G
|
XP_016869285.1:p.Tyr2624Cys
|
|
XM_017013797.1:c.7829A>G
|
XP_016869286.1:p.Tyr2610Cys
|
|
NM_003235.5:c.8090A>G
MANE Select
|
NP_003226.4:p.Tyr2697Cys
|
|