ENST00000374736.8:c.2297C>T
MANE Select
|
ENSP00000363868.3:p.Ala766Val
|
|
ENST00000678995.1:c.2297C>T
|
ENSP00000504612.1:p.Ala766Val
|
|
ENST00000374736.7:c.2297C>T
|
ENSP00000363868.3:p.Ala766Val
|
|
ENST00000494467.1:n.470C>T
|
|
|
NM_005502.3:c.2297C>T
|
NP_005493.2:p.Ala766Val
|
|
XM_005251773.1:c.2297C>T
|
XP_005251830.1:p.Ala766Val
|
|
XM_005251776.1:c.2117C>T
|
XP_005251833.1:p.Ala706Val
|
|
XM_011518339.1:c.2372C>T
|
XP_011516641.1:p.Ala791Val
|
|
XM_011518340.1:c.2372C>T
|
XP_011516642.1:p.Ala791Val
|
|
XM_011518341.1:c.2372C>T
|
XP_011516643.1:p.Ala791Val
|
|
XM_011518342.1:c.1934C>T
|
XP_011516644.1:p.Ala645Val
|
|
XM_011518343.1:c.2372C>T
|
XP_011516645.1:p.Ala791Val
|
|
XM_011518344.1:c.2372C>T
|
XP_011516646.1:p.Ala791Val
|
|
XM_005251773.3:c.2297C>T
|
XP_005251830.1:p.Ala766Val
|
|
XM_005251776.3:c.2117C>T
|
XP_005251833.1:p.Ala706Val
|
|
XM_011518339.3:c.2372C>T
|
XP_011516641.1:p.Ala791Val
|
|
XM_011518340.3:c.2372C>T
|
XP_011516642.1:p.Ala791Val
|
|
XM_011518341.3:c.2372C>T
|
XP_011516643.1:p.Ala791Val
|
|
XM_011518342.3:c.1934C>T
|
XP_011516644.1:p.Ala645Val
|
|
XM_011518344.2:c.2372C>T
|
XP_011516646.1:p.Ala791Val
|
|
XM_017014378.2:c.2372C>T
|
XP_016869867.1:p.Ala791Val
|
|
XM_017014379.2:c.2372C>T
|
XP_016869868.1:p.Ala791Val
|
|
XM_017014380.2:c.2372C>T
|
XP_016869869.1:p.Ala791Val
|
|
XM_017014381.2:c.2372C>T
|
XP_016869870.1:p.Ala791Val
|
|
XM_017014382.2:c.2234C>T
|
XP_016869871.1:p.Ala745Val
|
|
XR_001746223.1:n.2685C>T
|
|
|
NM_005502.4:c.2297C>T
MANE Select
|
NP_005493.2:p.Ala766Val
|
|