ENST00000220616.9:c.8003C>G
MANE Select
|
ENSP00000220616.4:p.Pro2668Arg
|
|
ENST00000220616.8:c.8003C>G
|
ENSP00000220616.4:p.Pro2668Arg
|
|
ENST00000519178.5:c.3369C>G
|
|
|
ENST00000519543.5:c.2402C>G
|
ENSP00000430430.1:p.Pro801Arg
|
|
ENST00000521107.1:c.215C>G
|
ENSP00000430161.1:p.Pro72Arg
|
|
ENST00000522691.1:n.89C>G
|
|
|
ENST00000523756.5:c.4658C>G
|
|
|
NM_003235.4:c.8003C>G
|
NP_003226.4:p.Pro2668Arg
|
|
XM_005251038.3:c.7811C>G
|
XP_005251095.1:p.Pro2604Arg
|
|
XM_006716622.2:c.7940C>G
|
XP_006716685.1:p.Pro2647Arg
|
|
XM_005251038.4:c.7811C>G
|
XP_005251095.1:p.Pro2604Arg
|
|
XM_006716622.3:c.7940C>G
|
XP_006716685.1:p.Pro2647Arg
|
|
XM_017013793.1:c.7937C>G
|
XP_016869282.1:p.Pro2646Arg
|
|
XM_017013794.1:c.7868C>G
|
XP_016869283.1:p.Pro2623Arg
|
|
XM_017013795.1:c.7832C>G
|
XP_016869284.1:p.Pro2611Arg
|
|
XM_017013796.1:c.7784C>G
|
XP_016869285.1:p.Pro2595Arg
|
|
XM_017013797.1:c.7742C>G
|
XP_016869286.1:p.Pro2581Arg
|
|
NM_003235.5:c.8003C>G
MANE Select
|
NP_003226.4:p.Pro2668Arg
|
|