ENST00000220616.9:c.8059G>T
MANE Select
|
ENSP00000220616.4:p.Asp2687Tyr
|
|
ENST00000220616.8:c.8059G>T
|
ENSP00000220616.4:p.Asp2687Tyr
|
|
ENST00000519178.5:c.3425G>T
|
|
|
ENST00000519543.5:c.2458G>T
|
ENSP00000430430.1:p.Asp820Tyr
|
|
ENST00000521107.1:c.271G>T
|
ENSP00000430161.1:p.Asp91Tyr
|
|
ENST00000522691.1:n.145G>T
|
|
|
ENST00000523756.5:c.4714G>T
|
|
|
NM_003235.4:c.8059G>T
|
NP_003226.4:p.Asp2687Tyr
|
|
XM_005251038.3:c.7867G>T
|
XP_005251095.1:p.Asp2623Tyr
|
|
XM_006716622.2:c.7996G>T
|
XP_006716685.1:p.Asp2666Tyr
|
|
XM_005251038.4:c.7867G>T
|
XP_005251095.1:p.Asp2623Tyr
|
|
XM_006716622.3:c.7996G>T
|
XP_006716685.1:p.Asp2666Tyr
|
|
XM_017013793.1:c.7993G>T
|
XP_016869282.1:p.Asp2665Tyr
|
|
XM_017013794.1:c.7924G>T
|
XP_016869283.1:p.Asp2642Tyr
|
|
XM_017013795.1:c.7888G>T
|
XP_016869284.1:p.Asp2630Tyr
|
|
XM_017013796.1:c.7840G>T
|
XP_016869285.1:p.Asp2614Tyr
|
|
XM_017013797.1:c.7798G>T
|
XP_016869286.1:p.Asp2600Tyr
|
|
NM_003235.5:c.8059G>T
MANE Select
|
NP_003226.4:p.Asp2687Tyr
|
|