ENST00000382103.7:c.365T>A
MANE Select
|
ENSP00000371535.2:p.Val122Asp
|
|
ENST00000680581.1:c.365T>A
|
ENSP00000506483.1:p.Val122Asp
|
|
ENST00000680824.1:n.1581T>A
|
|
|
ENST00000681071.1:n.657T>A
|
|
|
ENST00000681166.1:n.1412T>A
|
|
|
ENST00000681341.1:n.1506T>A
|
|
|
ENST00000681640.1:n.459T>A
|
|
|
ENST00000681948.1:c.620T>A
|
ENSP00000505991.1:p.Val207Asp
|
|
ENST00000358971.7:c.*163T>A
|
ENSP00000351857.3:n.*163T>A
|
|
ENST00000382103.6:c.365T>A
|
ENSP00000371535.2:p.Val122Asp
|
|
ENST00000514585.5:c.*66T>A
|
ENSP00000421880.1:n.*66T>A
|
|
NM_016955.3:c.365T>A
|
NP_058651.3:p.Val122Asp
|
|
XM_005248168.2:c.128T>A
|
XP_005248225.1:p.Val43Asp
|
|
XM_006713965.2:c.185T>A
|
XP_006714028.1:p.Val62Asp
|
|
XM_011513846.1:c.362T>A
|
XP_011512148.1:p.Val121Asp
|
|
XM_011513847.1:c.332T>A
|
XP_011512149.1:p.Val111Asp
|
|
XM_011513848.1:c.185T>A
|
XP_011512150.1:p.Val62Asp
|
|
XM_011513846.2:c.362T>A
|
XP_011512148.1:p.Val121Asp
|
|
XM_011513847.2:c.332T>A
|
XP_011512149.1:p.Val111Asp
|
|
XM_017008277.1:c.620T>A
|
XP_016863766.1:p.Val207Asp
|
|
XM_017008278.1:c.-59T>A
|
XP_016863767.1:n.-59T>A
|
|
NM_016955.4:c.365T>A
MANE Select
|
NP_058651.3:p.Val122Asp
|
|