ENST00000220616.9:c.8085G>T
MANE Select
|
ENSP00000220616.4:p.Glu2695Asp
|
|
ENST00000220616.8:c.8085G>T
|
ENSP00000220616.4:p.Glu2695Asp
|
|
ENST00000519178.5:c.3451G>T
|
|
|
ENST00000519543.5:c.2484G>T
|
ENSP00000430430.1:p.Glu828Asp
|
|
ENST00000521107.1:c.297G>T
|
ENSP00000430161.1:p.Glu99Asp
|
|
ENST00000522691.1:n.171G>T
|
|
|
ENST00000523756.5:c.4740G>T
|
|
|
NM_003235.4:c.8085G>T
|
NP_003226.4:p.Glu2695Asp
|
|
XM_005251038.3:c.7893G>T
|
XP_005251095.1:p.Glu2631Asp
|
|
XM_006716622.2:c.8022G>T
|
XP_006716685.1:p.Glu2674Asp
|
|
XM_005251038.4:c.7893G>T
|
XP_005251095.1:p.Glu2631Asp
|
|
XM_006716622.3:c.8022G>T
|
XP_006716685.1:p.Glu2674Asp
|
|
XM_017013793.1:c.8019G>T
|
XP_016869282.1:p.Glu2673Asp
|
|
XM_017013794.1:c.7950G>T
|
XP_016869283.1:p.Glu2650Asp
|
|
XM_017013795.1:c.7914G>T
|
XP_016869284.1:p.Glu2638Asp
|
|
XM_017013796.1:c.7866G>T
|
XP_016869285.1:p.Glu2622Asp
|
|
XM_017013797.1:c.7824G>T
|
XP_016869286.1:p.Glu2608Asp
|
|
NM_003235.5:c.8085G>T
MANE Select
|
NP_003226.4:p.Glu2695Asp
|
|