ENST00000220616.9:c.8057C>A
MANE Select
|
ENSP00000220616.4:p.Pro2686His
|
|
ENST00000220616.8:c.8057C>A
|
ENSP00000220616.4:p.Pro2686His
|
|
ENST00000519178.5:c.3423C>A
|
|
|
ENST00000519543.5:c.2456C>A
|
ENSP00000430430.1:p.Pro819His
|
|
ENST00000521107.1:c.269C>A
|
ENSP00000430161.1:p.Pro90His
|
|
ENST00000522691.1:n.143C>A
|
|
|
ENST00000523756.5:c.4712C>A
|
|
|
NM_003235.4:c.8057C>A
|
NP_003226.4:p.Pro2686His
|
|
XM_005251038.3:c.7865C>A
|
XP_005251095.1:p.Pro2622His
|
|
XM_006716622.2:c.7994C>A
|
XP_006716685.1:p.Pro2665His
|
|
XM_005251038.4:c.7865C>A
|
XP_005251095.1:p.Pro2622His
|
|
XM_006716622.3:c.7994C>A
|
XP_006716685.1:p.Pro2665His
|
|
XM_017013793.1:c.7991C>A
|
XP_016869282.1:p.Pro2664His
|
|
XM_017013794.1:c.7922C>A
|
XP_016869283.1:p.Pro2641His
|
|
XM_017013795.1:c.7886C>A
|
XP_016869284.1:p.Pro2629His
|
|
XM_017013796.1:c.7838C>A
|
XP_016869285.1:p.Pro2613His
|
|
XM_017013797.1:c.7796C>A
|
XP_016869286.1:p.Pro2599His
|
|
NM_003235.5:c.8057C>A
MANE Select
|
NP_003226.4:p.Pro2686His
|
|