ENST00000399503.4:c.2708A>T
MANE Select
|
ENSP00000382423.3:p.Glu903Val
|
|
ENST00000399503.3:c.2708A>T
|
ENSP00000382423.3:p.Glu903Val
|
|
NM_005921.1:c.2708A>T
|
NP_005912.1:p.Glu903Val
|
|
XM_005248519.3:c.2330A>T
|
XP_005248576.2:p.Glu777Val
|
|
XM_011543406.1:c.2453A>T
|
XP_011541708.1:p.Glu818Val
|
|
XM_011543407.1:c.2429A>T
|
XP_011541709.1:p.Glu810Val
|
|
XM_011543408.1:c.2708A>T
|
XP_011541710.1:p.Glu903Val
|
|
XM_017009484.1:c.2297A>T
|
XP_016864973.1:p.Glu766Val
|
|
XM_017009485.1:c.2219A>T
|
XP_016864974.1:p.Glu740Val
|
|
XR_001742068.2:n.2739A>T
|
|
|
NM_005921.2:c.2708A>T
MANE Select
|
NP_005912.1:p.Glu903Val
|
|