ENST00000220616.9:c.8126G>A
MANE Select
|
ENSP00000220616.4:p.Gly2709Asp
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|
ENST00000220616.8:c.8126G>A
|
ENSP00000220616.4:p.Gly2709Asp
|
|
ENST00000519178.5:c.3492G>A
|
|
|
ENST00000519543.5:c.2525G>A
|
ENSP00000430430.1:p.Gly842Asp
|
|
ENST00000521107.1:c.338G>A
|
ENSP00000430161.1:p.Gly113Asp
|
|
ENST00000522691.1:n.212G>A
|
|
|
ENST00000523756.5:c.4781G>A
|
|
|
NM_003235.4:c.8126G>A
|
NP_003226.4:p.Gly2709Asp
|
|
XM_005251038.3:c.7934G>A
|
XP_005251095.1:p.Gly2645Asp
|
|
XM_006716622.2:c.8063G>A
|
XP_006716685.1:p.Gly2688Asp
|
|
XM_005251038.4:c.7934G>A
|
XP_005251095.1:p.Gly2645Asp
|
|
XM_006716622.3:c.8063G>A
|
XP_006716685.1:p.Gly2688Asp
|
|
XM_017013793.1:c.8060G>A
|
XP_016869282.1:p.Gly2687Asp
|
|
XM_017013794.1:c.7991G>A
|
XP_016869283.1:p.Gly2664Asp
|
|
XM_017013795.1:c.7955G>A
|
XP_016869284.1:p.Gly2652Asp
|
|
XM_017013796.1:c.7907G>A
|
XP_016869285.1:p.Gly2636Asp
|
|
XM_017013797.1:c.7865G>A
|
XP_016869286.1:p.Gly2622Asp
|
|
NM_003235.5:c.8126G>A
MANE Select
|
NP_003226.4:p.Gly2709Asp
|
|