ENST00000220616.9:c.8097G>T
MANE Select
|
ENSP00000220616.4:p.Glu2699Asp
|
|
ENST00000220616.8:c.8097G>T
|
ENSP00000220616.4:p.Glu2699Asp
|
|
ENST00000519178.5:c.3463G>T
|
|
|
ENST00000519543.5:c.2496G>T
|
ENSP00000430430.1:p.Glu832Asp
|
|
ENST00000521107.1:c.309G>T
|
ENSP00000430161.1:p.Glu103Asp
|
|
ENST00000522691.1:n.183G>T
|
|
|
ENST00000523756.5:c.4752G>T
|
|
|
NM_003235.4:c.8097G>T
|
NP_003226.4:p.Glu2699Asp
|
|
XM_005251038.3:c.7905G>T
|
XP_005251095.1:p.Glu2635Asp
|
|
XM_006716622.2:c.8034G>T
|
XP_006716685.1:p.Glu2678Asp
|
|
XM_005251038.4:c.7905G>T
|
XP_005251095.1:p.Glu2635Asp
|
|
XM_006716622.3:c.8034G>T
|
XP_006716685.1:p.Glu2678Asp
|
|
XM_017013793.1:c.8031G>T
|
XP_016869282.1:p.Glu2677Asp
|
|
XM_017013794.1:c.7962G>T
|
XP_016869283.1:p.Glu2654Asp
|
|
XM_017013795.1:c.7926G>T
|
XP_016869284.1:p.Glu2642Asp
|
|
XM_017013796.1:c.7878G>T
|
XP_016869285.1:p.Glu2626Asp
|
|
XM_017013797.1:c.7836G>T
|
XP_016869286.1:p.Glu2612Asp
|
|
NM_003235.5:c.8097G>T
MANE Select
|
NP_003226.4:p.Glu2699Asp
|
|