ENST00000220616.9:c.8116A>C
MANE Select
|
ENSP00000220616.4:p.Asn2706His
|
|
ENST00000220616.8:c.8116A>C
|
ENSP00000220616.4:p.Asn2706His
|
|
ENST00000519178.5:c.3482A>C
|
|
|
ENST00000519543.5:c.2515A>C
|
ENSP00000430430.1:p.Asn839His
|
|
ENST00000521107.1:c.328A>C
|
ENSP00000430161.1:p.Asn110His
|
|
ENST00000522691.1:n.202A>C
|
|
|
ENST00000523756.5:c.4771A>C
|
|
|
NM_003235.4:c.8116A>C
|
NP_003226.4:p.Asn2706His
|
|
XM_005251038.3:c.7924A>C
|
XP_005251095.1:p.Asn2642His
|
|
XM_006716622.2:c.8053A>C
|
XP_006716685.1:p.Asn2685His
|
|
XM_005251038.4:c.7924A>C
|
XP_005251095.1:p.Asn2642His
|
|
XM_006716622.3:c.8053A>C
|
XP_006716685.1:p.Asn2685His
|
|
XM_017013793.1:c.8050A>C
|
XP_016869282.1:p.Asn2684His
|
|
XM_017013794.1:c.7981A>C
|
XP_016869283.1:p.Asn2661His
|
|
XM_017013795.1:c.7945A>C
|
XP_016869284.1:p.Asn2649His
|
|
XM_017013796.1:c.7897A>C
|
XP_016869285.1:p.Asn2633His
|
|
XM_017013797.1:c.7855A>C
|
XP_016869286.1:p.Asn2619His
|
|
NM_003235.5:c.8116A>C
MANE Select
|
NP_003226.4:p.Asn2706His
|
|