ENST00000220616.9:c.8114C>G
MANE Select
|
ENSP00000220616.4:p.Pro2705Arg
|
|
ENST00000220616.8:c.8114C>G
|
ENSP00000220616.4:p.Pro2705Arg
|
|
ENST00000519178.5:c.3480C>G
|
|
|
ENST00000519543.5:c.2513C>G
|
ENSP00000430430.1:p.Pro838Arg
|
|
ENST00000521107.1:c.326C>G
|
ENSP00000430161.1:p.Pro109Arg
|
|
ENST00000522691.1:n.200C>G
|
|
|
ENST00000523756.5:c.4769C>G
|
|
|
NM_003235.4:c.8114C>G
|
NP_003226.4:p.Pro2705Arg
|
|
XM_005251038.3:c.7922C>G
|
XP_005251095.1:p.Pro2641Arg
|
|
XM_006716622.2:c.8051C>G
|
XP_006716685.1:p.Pro2684Arg
|
|
XM_005251038.4:c.7922C>G
|
XP_005251095.1:p.Pro2641Arg
|
|
XM_006716622.3:c.8051C>G
|
XP_006716685.1:p.Pro2684Arg
|
|
XM_017013793.1:c.8048C>G
|
XP_016869282.1:p.Pro2683Arg
|
|
XM_017013794.1:c.7979C>G
|
XP_016869283.1:p.Pro2660Arg
|
|
XM_017013795.1:c.7943C>G
|
XP_016869284.1:p.Pro2648Arg
|
|
XM_017013796.1:c.7895C>G
|
XP_016869285.1:p.Pro2632Arg
|
|
XM_017013797.1:c.7853C>G
|
XP_016869286.1:p.Pro2618Arg
|
|
NM_003235.5:c.8114C>G
MANE Select
|
NP_003226.4:p.Pro2705Arg
|
|