ENST00000220616.9:c.8116A>T
MANE Select
|
ENSP00000220616.4:p.Asn2706Tyr
|
|
ENST00000220616.8:c.8116A>T
|
ENSP00000220616.4:p.Asn2706Tyr
|
|
ENST00000519178.5:c.3482A>T
|
|
|
ENST00000519543.5:c.2515A>T
|
ENSP00000430430.1:p.Asn839Tyr
|
|
ENST00000521107.1:c.328A>T
|
ENSP00000430161.1:p.Asn110Tyr
|
|
ENST00000522691.1:n.202A>T
|
|
|
ENST00000523756.5:c.4771A>T
|
|
|
NM_003235.4:c.8116A>T
|
NP_003226.4:p.Asn2706Tyr
|
|
XM_005251038.3:c.7924A>T
|
XP_005251095.1:p.Asn2642Tyr
|
|
XM_006716622.2:c.8053A>T
|
XP_006716685.1:p.Asn2685Tyr
|
|
XM_005251038.4:c.7924A>T
|
XP_005251095.1:p.Asn2642Tyr
|
|
XM_006716622.3:c.8053A>T
|
XP_006716685.1:p.Asn2685Tyr
|
|
XM_017013793.1:c.8050A>T
|
XP_016869282.1:p.Asn2684Tyr
|
|
XM_017013794.1:c.7981A>T
|
XP_016869283.1:p.Asn2661Tyr
|
|
XM_017013795.1:c.7945A>T
|
XP_016869284.1:p.Asn2649Tyr
|
|
XM_017013796.1:c.7897A>T
|
XP_016869285.1:p.Asn2633Tyr
|
|
XM_017013797.1:c.7855A>T
|
XP_016869286.1:p.Asn2619Tyr
|
|
NM_003235.5:c.8116A>T
MANE Select
|
NP_003226.4:p.Asn2706Tyr
|
|