ENST00000220616.9:c.8116A>G
MANE Select
|
ENSP00000220616.4:p.Asn2706Asp
|
|
ENST00000220616.8:c.8116A>G
|
ENSP00000220616.4:p.Asn2706Asp
|
|
ENST00000519178.5:c.3482A>G
|
|
|
ENST00000519543.5:c.2515A>G
|
ENSP00000430430.1:p.Asn839Asp
|
|
ENST00000521107.1:c.328A>G
|
ENSP00000430161.1:p.Asn110Asp
|
|
ENST00000522691.1:n.202A>G
|
|
|
ENST00000523756.5:c.4771A>G
|
|
|
NM_003235.4:c.8116A>G
|
NP_003226.4:p.Asn2706Asp
|
|
XM_005251038.3:c.7924A>G
|
XP_005251095.1:p.Asn2642Asp
|
|
XM_006716622.2:c.8053A>G
|
XP_006716685.1:p.Asn2685Asp
|
|
XM_005251038.4:c.7924A>G
|
XP_005251095.1:p.Asn2642Asp
|
|
XM_006716622.3:c.8053A>G
|
XP_006716685.1:p.Asn2685Asp
|
|
XM_017013793.1:c.8050A>G
|
XP_016869282.1:p.Asn2684Asp
|
|
XM_017013794.1:c.7981A>G
|
XP_016869283.1:p.Asn2661Asp
|
|
XM_017013795.1:c.7945A>G
|
XP_016869284.1:p.Asn2649Asp
|
|
XM_017013796.1:c.7897A>G
|
XP_016869285.1:p.Asn2633Asp
|
|
XM_017013797.1:c.7855A>G
|
XP_016869286.1:p.Asn2619Asp
|
|
NM_003235.5:c.8116A>G
MANE Select
|
NP_003226.4:p.Asn2706Asp
|
|