ENST00000220616.9:c.8147C>A
MANE Select
|
ENSP00000220616.4:p.Ser2716Tyr
|
|
ENST00000220616.8:c.8147C>A
|
ENSP00000220616.4:p.Ser2716Tyr
|
|
ENST00000519178.5:c.3513C>A
|
|
|
ENST00000519543.5:c.2546C>A
|
ENSP00000430430.1:p.Ser849Tyr
|
|
ENST00000521107.1:c.359C>A
|
ENSP00000430161.1:p.Ser120Tyr
|
|
ENST00000522691.1:n.233C>A
|
|
|
ENST00000523756.5:c.4802C>A
|
|
|
NM_003235.4:c.8147C>A
|
NP_003226.4:p.Ser2716Tyr
|
|
XM_005251038.3:c.7955C>A
|
XP_005251095.1:p.Ser2652Tyr
|
|
XM_006716622.2:c.8084C>A
|
XP_006716685.1:p.Ser2695Tyr
|
|
XM_005251038.4:c.7955C>A
|
XP_005251095.1:p.Ser2652Tyr
|
|
XM_006716622.3:c.8084C>A
|
XP_006716685.1:p.Ser2695Tyr
|
|
XM_017013793.1:c.8081C>A
|
XP_016869282.1:p.Ser2694Tyr
|
|
XM_017013794.1:c.8012C>A
|
XP_016869283.1:p.Ser2671Tyr
|
|
XM_017013795.1:c.7976C>A
|
XP_016869284.1:p.Ser2659Tyr
|
|
XM_017013796.1:c.7928C>A
|
XP_016869285.1:p.Ser2643Tyr
|
|
XM_017013797.1:c.7886C>A
|
XP_016869286.1:p.Ser2629Tyr
|
|
NM_003235.5:c.8147C>A
MANE Select
|
NP_003226.4:p.Ser2716Tyr
|
|