ENST00000220616.9:c.8182T>G
MANE Select
|
ENSP00000220616.4:p.Ser2728Ala
|
|
ENST00000220616.8:c.8182T>G
|
ENSP00000220616.4:p.Ser2728Ala
|
|
ENST00000519178.5:c.3548T>G
|
|
|
ENST00000519543.5:c.2581T>G
|
ENSP00000430430.1:p.Ser861Ala
|
|
ENST00000521107.1:c.394T>G
|
ENSP00000430161.1:p.Ser132Ala
|
|
ENST00000522691.1:n.268T>G
|
|
|
ENST00000523756.5:c.4837T>G
|
|
|
NM_003235.4:c.8182T>G
|
NP_003226.4:p.Ser2728Ala
|
|
XM_005251038.3:c.7990T>G
|
XP_005251095.1:p.Ser2664Ala
|
|
XM_006716622.2:c.8119T>G
|
XP_006716685.1:p.Ser2707Ala
|
|
XM_005251038.4:c.7990T>G
|
XP_005251095.1:p.Ser2664Ala
|
|
XM_006716622.3:c.8119T>G
|
XP_006716685.1:p.Ser2707Ala
|
|
XM_017013793.1:c.8116T>G
|
XP_016869282.1:p.Ser2706Ala
|
|
XM_017013794.1:c.8047T>G
|
XP_016869283.1:p.Ser2683Ala
|
|
XM_017013795.1:c.8011T>G
|
XP_016869284.1:p.Ser2671Ala
|
|
XM_017013796.1:c.7963T>G
|
XP_016869285.1:p.Ser2655Ala
|
|
XM_017013797.1:c.7921T>G
|
XP_016869286.1:p.Ser2641Ala
|
|
NM_003235.5:c.8182T>G
MANE Select
|
NP_003226.4:p.Ser2728Ala
|
|