ENST00000220616.9:c.8037C>A
MANE Select
|
ENSP00000220616.4:p.Pro2679=
|
|
ENST00000220616.8:c.8037C>A
|
ENSP00000220616.4:p.Pro2679=
|
|
ENST00000519178.5:c.3403C>A
|
|
|
ENST00000519543.5:c.2436C>A
|
ENSP00000430430.1:p.Pro812=
|
|
ENST00000521107.1:c.249C>A
|
ENSP00000430161.1:p.Pro83=
|
|
ENST00000522691.1:n.123C>A
|
|
|
ENST00000523756.5:c.4692C>A
|
|
|
NM_003235.4:c.8037C>A
|
NP_003226.4:p.Pro2679=
|
|
XM_005251038.3:c.7845C>A
|
XP_005251095.1:p.Pro2615=
|
|
XM_006716622.2:c.7974C>A
|
XP_006716685.1:p.Pro2658=
|
|
XM_005251038.4:c.7845C>A
|
XP_005251095.1:p.Pro2615=
|
|
XM_006716622.3:c.7974C>A
|
XP_006716685.1:p.Pro2658=
|
|
XM_017013793.1:c.7971C>A
|
XP_016869282.1:p.Pro2657=
|
|
XM_017013794.1:c.7902C>A
|
XP_016869283.1:p.Pro2634=
|
|
XM_017013795.1:c.7866C>A
|
XP_016869284.1:p.Pro2622=
|
|
XM_017013796.1:c.7818C>A
|
XP_016869285.1:p.Pro2606=
|
|
XM_017013797.1:c.7776C>A
|
XP_016869286.1:p.Pro2592=
|
|
NM_003235.5:c.8037C>A
MANE Select
|
NP_003226.4:p.Pro2679=
|
|