ENST00000374736.8:c.4991C>T
MANE Select
|
ENSP00000363868.3:p.Ala1664Val
|
|
ENST00000678995.1:c.4997C>T
|
ENSP00000504612.1:p.Ala1666Val
|
|
ENST00000374736.7:c.4991C>T
|
ENSP00000363868.3:p.Ala1664Val
|
|
NM_005502.3:c.4991C>T
|
NP_005493.2:p.Ala1664Val
|
|
XM_005251773.1:c.4997C>T
|
XP_005251830.1:p.Ala1666Val
|
|
XM_005251776.1:c.4817C>T
|
XP_005251833.1:p.Ala1606Val
|
|
XM_011518339.1:c.5072C>T
|
XP_011516641.1:p.Ala1691Val
|
|
XM_011518340.1:c.5072C>T
|
XP_011516642.1:p.Ala1691Val
|
|
XM_011518341.1:c.5066C>T
|
XP_011516643.1:p.Ala1689Val
|
|
XM_011518342.1:c.4634C>T
|
XP_011516644.1:p.Ala1545Val
|
|
XM_011518343.1:c.5072C>T
|
XP_011516645.1:p.Ala1691Val
|
|
XM_005251773.3:c.4997C>T
|
XP_005251830.1:p.Ala1666Val
|
|
XM_005251776.3:c.4817C>T
|
XP_005251833.1:p.Ala1606Val
|
|
XM_011518339.3:c.5072C>T
|
XP_011516641.1:p.Ala1691Val
|
|
XM_011518340.3:c.5072C>T
|
XP_011516642.1:p.Ala1691Val
|
|
XM_011518341.3:c.5066C>T
|
XP_011516643.1:p.Ala1689Val
|
|
XM_011518342.3:c.4634C>T
|
XP_011516644.1:p.Ala1545Val
|
|
XM_017014378.2:c.5072C>T
|
XP_016869867.1:p.Ala1691Val
|
|
XM_017014379.2:c.5072C>T
|
XP_016869868.1:p.Ala1691Val
|
|
XM_017014380.2:c.5072C>T
|
XP_016869869.1:p.Ala1691Val
|
|
XM_017014381.2:c.5072C>T
|
XP_016869870.1:p.Ala1691Val
|
|
XM_017014382.2:c.4934C>T
|
XP_016869871.1:p.Ala1645Val
|
|
XR_001746223.1:n.5385C>T
|
|
|
NM_005502.4:c.4991C>T
MANE Select
|
NP_005493.2:p.Ala1664Val
|
|