ENST00000264499.9:c.1976A>T
MANE Select
|
ENSP00000264499.4:p.Glu659Val
|
|
ENST00000264499.8:c.1976A>T
|
ENSP00000264499.4:p.Glu659Val
|
|
ENST00000506636.1:c.1976A>T
|
ENSP00000423626.1:p.Glu659Val
|
|
ENST00000507814.5:c.245A>T
|
ENSP00000423250.1:p.Glu82Val
|
|
NM_018190.3:c.1976A>T
|
NP_060660.2:p.Glu659Val
|
|
NM_176824.2:c.1976A>T
|
NP_789794.1:p.Glu659Val
|
|
XM_005263106.2:c.1979A>T
|
XP_005263163.1:p.Glu660Val
|
|
XM_011532079.1:c.2024A>T
|
XP_011530381.1:p.Glu675Val
|
|
XM_011532080.1:c.2021A>T
|
XP_011530382.1:p.Glu674Val
|
|
XM_011532081.1:c.1859A>T
|
XP_011530383.1:p.Glu620Val
|
|
XM_005263106.4:c.1979A>T
|
XP_005263163.1:p.Glu660Val
|
|
XM_011532079.3:c.2024A>T
|
XP_011530381.1:p.Glu675Val
|
|
XM_011532080.3:c.2021A>T
|
XP_011530382.1:p.Glu674Val
|
|
XM_011532081.3:c.1859A>T
|
XP_011530383.1:p.Glu620Val
|
|
XM_017008357.2:c.1811A>T
|
XP_016863846.1:p.Glu604Val
|
|
XM_017008358.2:c.1814A>T
|
XP_016863847.1:p.Glu605Val
|
|
NM_176824.3:c.1976A>T
MANE Select
|
NP_789794.1:p.Glu659Val
|
|
NM_018190.4:c.1976A>T
|
NP_060660.2:p.Glu659Val
|
|