ENST00000220616.9:c.8075C>A
MANE Select
|
ENSP00000220616.4:p.Ala2692Asp
|
|
ENST00000220616.8:c.8075C>A
|
ENSP00000220616.4:p.Ala2692Asp
|
|
ENST00000519178.5:c.3441C>A
|
|
|
ENST00000519543.5:c.2474C>A
|
ENSP00000430430.1:p.Ala825Asp
|
|
ENST00000521107.1:c.287C>A
|
ENSP00000430161.1:p.Ala96Asp
|
|
ENST00000522691.1:n.161C>A
|
|
|
ENST00000523756.5:c.4730C>A
|
|
|
NM_003235.4:c.8075C>A
|
NP_003226.4:p.Ala2692Asp
|
|
XM_005251038.3:c.7883C>A
|
XP_005251095.1:p.Ala2628Asp
|
|
XM_006716622.2:c.8012C>A
|
XP_006716685.1:p.Ala2671Asp
|
|
XM_005251038.4:c.7883C>A
|
XP_005251095.1:p.Ala2628Asp
|
|
XM_006716622.3:c.8012C>A
|
XP_006716685.1:p.Ala2671Asp
|
|
XM_017013793.1:c.8009C>A
|
XP_016869282.1:p.Ala2670Asp
|
|
XM_017013794.1:c.7940C>A
|
XP_016869283.1:p.Ala2647Asp
|
|
XM_017013795.1:c.7904C>A
|
XP_016869284.1:p.Ala2635Asp
|
|
XM_017013796.1:c.7856C>A
|
XP_016869285.1:p.Ala2619Asp
|
|
XM_017013797.1:c.7814C>A
|
XP_016869286.1:p.Ala2605Asp
|
|
NM_003235.5:c.8075C>A
MANE Select
|
NP_003226.4:p.Ala2692Asp
|
|