ENST00000220616.9:c.8069C>G
MANE Select
|
ENSP00000220616.4:p.Pro2690Arg
|
|
ENST00000220616.8:c.8069C>G
|
ENSP00000220616.4:p.Pro2690Arg
|
|
ENST00000519178.5:c.3435C>G
|
|
|
ENST00000519543.5:c.2468C>G
|
ENSP00000430430.1:p.Pro823Arg
|
|
ENST00000521107.1:c.281C>G
|
ENSP00000430161.1:p.Pro94Arg
|
|
ENST00000522691.1:n.155C>G
|
|
|
ENST00000523756.5:c.4724C>G
|
|
|
NM_003235.4:c.8069C>G
|
NP_003226.4:p.Pro2690Arg
|
|
XM_005251038.3:c.7877C>G
|
XP_005251095.1:p.Pro2626Arg
|
|
XM_006716622.2:c.8006C>G
|
XP_006716685.1:p.Pro2669Arg
|
|
XM_005251038.4:c.7877C>G
|
XP_005251095.1:p.Pro2626Arg
|
|
XM_006716622.3:c.8006C>G
|
XP_006716685.1:p.Pro2669Arg
|
|
XM_017013793.1:c.8003C>G
|
XP_016869282.1:p.Pro2668Arg
|
|
XM_017013794.1:c.7934C>G
|
XP_016869283.1:p.Pro2645Arg
|
|
XM_017013795.1:c.7898C>G
|
XP_016869284.1:p.Pro2633Arg
|
|
XM_017013796.1:c.7850C>G
|
XP_016869285.1:p.Pro2617Arg
|
|
XM_017013797.1:c.7808C>G
|
XP_016869286.1:p.Pro2603Arg
|
|
NM_003235.5:c.8069C>G
MANE Select
|
NP_003226.4:p.Pro2690Arg
|
|