ENST00000382103.7:c.377T>G
MANE Select
|
ENSP00000371535.2:p.Ile126Arg
|
|
ENST00000680581.1:c.377T>G
|
ENSP00000506483.1:p.Ile126Arg
|
|
ENST00000680824.1:n.1593T>G
|
|
|
ENST00000681071.1:n.669T>G
|
|
|
ENST00000681166.1:n.1424T>G
|
|
|
ENST00000681341.1:n.1518T>G
|
|
|
ENST00000681640.1:n.471T>G
|
|
|
ENST00000681948.1:c.632T>G
|
ENSP00000505991.1:p.Ile211Arg
|
|
ENST00000358971.7:c.*175T>G
|
ENSP00000351857.3:n.*175T>G
|
|
ENST00000382103.6:c.377T>G
|
ENSP00000371535.2:p.Ile126Arg
|
|
ENST00000514585.5:c.*78T>G
|
ENSP00000421880.1:n.*78T>G
|
|
NM_016955.3:c.377T>G
|
NP_058651.3:p.Ile126Arg
|
|
XM_005248168.2:c.140T>G
|
XP_005248225.1:p.Ile47Arg
|
|
XM_006713965.2:c.197T>G
|
XP_006714028.1:p.Ile66Arg
|
|
XM_011513846.1:c.374T>G
|
XP_011512148.1:p.Ile125Arg
|
|
XM_011513847.1:c.344T>G
|
XP_011512149.1:p.Ile115Arg
|
|
XM_011513848.1:c.197T>G
|
XP_011512150.1:p.Ile66Arg
|
|
XM_011513846.2:c.374T>G
|
XP_011512148.1:p.Ile125Arg
|
|
XM_011513847.2:c.344T>G
|
XP_011512149.1:p.Ile115Arg
|
|
XM_017008277.1:c.632T>G
|
XP_016863766.1:p.Ile211Arg
|
|
XM_017008278.1:c.-47T>G
|
XP_016863767.1:n.-47T>G
|
|
NM_016955.4:c.377T>G
MANE Select
|
NP_058651.3:p.Ile126Arg
|
|