ENST00000220616.9:c.8052C>A
MANE Select
|
ENSP00000220616.4:p.Pro2684=
|
|
ENST00000220616.8:c.8052C>A
|
ENSP00000220616.4:p.Pro2684=
|
|
ENST00000519178.5:c.3418C>A
|
|
|
ENST00000519543.5:c.2451C>A
|
ENSP00000430430.1:p.Pro817=
|
|
ENST00000521107.1:c.264C>A
|
ENSP00000430161.1:p.Pro88=
|
|
ENST00000522691.1:n.138C>A
|
|
|
ENST00000523756.5:c.4707C>A
|
|
|
NM_003235.4:c.8052C>A
|
NP_003226.4:p.Pro2684=
|
|
XM_005251038.3:c.7860C>A
|
XP_005251095.1:p.Pro2620=
|
|
XM_006716622.2:c.7989C>A
|
XP_006716685.1:p.Pro2663=
|
|
XM_005251038.4:c.7860C>A
|
XP_005251095.1:p.Pro2620=
|
|
XM_006716622.3:c.7989C>A
|
XP_006716685.1:p.Pro2663=
|
|
XM_017013793.1:c.7986C>A
|
XP_016869282.1:p.Pro2662=
|
|
XM_017013794.1:c.7917C>A
|
XP_016869283.1:p.Pro2639=
|
|
XM_017013795.1:c.7881C>A
|
XP_016869284.1:p.Pro2627=
|
|
XM_017013796.1:c.7833C>A
|
XP_016869285.1:p.Pro2611=
|
|
XM_017013797.1:c.7791C>A
|
XP_016869286.1:p.Pro2597=
|
|
NM_003235.5:c.8052C>A
MANE Select
|
NP_003226.4:p.Pro2684=
|
|