ENST00000220616.9:c.8056C>G
MANE Select
|
ENSP00000220616.4:p.Pro2686Ala
|
|
ENST00000220616.8:c.8056C>G
|
ENSP00000220616.4:p.Pro2686Ala
|
|
ENST00000519178.5:c.3422C>G
|
|
|
ENST00000519543.5:c.2455C>G
|
ENSP00000430430.1:p.Pro819Ala
|
|
ENST00000521107.1:c.268C>G
|
ENSP00000430161.1:p.Pro90Ala
|
|
ENST00000522691.1:n.142C>G
|
|
|
ENST00000523756.5:c.4711C>G
|
|
|
NM_003235.4:c.8056C>G
|
NP_003226.4:p.Pro2686Ala
|
|
XM_005251038.3:c.7864C>G
|
XP_005251095.1:p.Pro2622Ala
|
|
XM_006716622.2:c.7993C>G
|
XP_006716685.1:p.Pro2665Ala
|
|
XM_005251038.4:c.7864C>G
|
XP_005251095.1:p.Pro2622Ala
|
|
XM_006716622.3:c.7993C>G
|
XP_006716685.1:p.Pro2665Ala
|
|
XM_017013793.1:c.7990C>G
|
XP_016869282.1:p.Pro2664Ala
|
|
XM_017013794.1:c.7921C>G
|
XP_016869283.1:p.Pro2641Ala
|
|
XM_017013795.1:c.7885C>G
|
XP_016869284.1:p.Pro2629Ala
|
|
XM_017013796.1:c.7837C>G
|
XP_016869285.1:p.Pro2613Ala
|
|
XM_017013797.1:c.7795C>G
|
XP_016869286.1:p.Pro2599Ala
|
|
NM_003235.5:c.8056C>G
MANE Select
|
NP_003226.4:p.Pro2686Ala
|
|