ENST00000220616.9:c.8086A>G
MANE Select
|
ENSP00000220616.4:p.Asn2696Asp
|
|
ENST00000220616.8:c.8086A>G
|
ENSP00000220616.4:p.Asn2696Asp
|
|
ENST00000519178.5:c.3452A>G
|
|
|
ENST00000519543.5:c.2485A>G
|
ENSP00000430430.1:p.Asn829Asp
|
|
ENST00000521107.1:c.298A>G
|
ENSP00000430161.1:p.Asn100Asp
|
|
ENST00000522691.1:n.172A>G
|
|
|
ENST00000523756.5:c.4741A>G
|
|
|
NM_003235.4:c.8086A>G
|
NP_003226.4:p.Asn2696Asp
|
|
XM_005251038.3:c.7894A>G
|
XP_005251095.1:p.Asn2632Asp
|
|
XM_006716622.2:c.8023A>G
|
XP_006716685.1:p.Asn2675Asp
|
|
XM_005251038.4:c.7894A>G
|
XP_005251095.1:p.Asn2632Asp
|
|
XM_006716622.3:c.8023A>G
|
XP_006716685.1:p.Asn2675Asp
|
|
XM_017013793.1:c.8020A>G
|
XP_016869282.1:p.Asn2674Asp
|
|
XM_017013794.1:c.7951A>G
|
XP_016869283.1:p.Asn2651Asp
|
|
XM_017013795.1:c.7915A>G
|
XP_016869284.1:p.Asn2639Asp
|
|
XM_017013796.1:c.7867A>G
|
XP_016869285.1:p.Asn2623Asp
|
|
XM_017013797.1:c.7825A>G
|
XP_016869286.1:p.Asn2609Asp
|
|
NM_003235.5:c.8086A>G
MANE Select
|
NP_003226.4:p.Asn2696Asp
|
|