ENST00000220616.9:c.8105A>T
MANE Select
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ENSP00000220616.4:p.Glu2702Val
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ENST00000220616.8:c.8105A>T
|
ENSP00000220616.4:p.Glu2702Val
|
|
ENST00000519178.5:c.3471A>T
|
|
|
ENST00000519543.5:c.2504A>T
|
ENSP00000430430.1:p.Glu835Val
|
|
ENST00000521107.1:c.317A>T
|
ENSP00000430161.1:p.Glu106Val
|
|
ENST00000522691.1:n.191A>T
|
|
|
ENST00000523756.5:c.4760A>T
|
|
|
NM_003235.4:c.8105A>T
|
NP_003226.4:p.Glu2702Val
|
|
XM_005251038.3:c.7913A>T
|
XP_005251095.1:p.Glu2638Val
|
|
XM_006716622.2:c.8042A>T
|
XP_006716685.1:p.Glu2681Val
|
|
XM_005251038.4:c.7913A>T
|
XP_005251095.1:p.Glu2638Val
|
|
XM_006716622.3:c.8042A>T
|
XP_006716685.1:p.Glu2681Val
|
|
XM_017013793.1:c.8039A>T
|
XP_016869282.1:p.Glu2680Val
|
|
XM_017013794.1:c.7970A>T
|
XP_016869283.1:p.Glu2657Val
|
|
XM_017013795.1:c.7934A>T
|
XP_016869284.1:p.Glu2645Val
|
|
XM_017013796.1:c.7886A>T
|
XP_016869285.1:p.Glu2629Val
|
|
XM_017013797.1:c.7844A>T
|
XP_016869286.1:p.Glu2615Val
|
|
NM_003235.5:c.8105A>T
MANE Select
|
NP_003226.4:p.Glu2702Val
|
|