|
NM_000442.5:c.373G=
MANE Select
|
NP_000433.4:p.Val125=
|
|
ENST00000563924.6:c.373G=
MANE Select
|
ENSP00000457421.1:p.Val125=
|
|
NM_000442.4:c.373G=
|
NP_000433.4:p.Val125=
|
|
ENST00000561739.5:n.402G=
|
|
|
ENST00000563523.5:c.358G=
|
ENSP00000455931.1:p.Val120=
|
|
ENST00000563924.5:c.373G=
|
ENSP00000457421.1:p.Val125=
|
|
ENST00000564866.5:c.373G=
|
ENSP00000455663.1:p.Val125=
|
|
ENST00000566616.1:n.352G=
|
|
|
ENST00000569530.1:n.359G=
|
|
|
ENST00000569967.1:c.373G=
|
ENSP00000457218.1:p.Val125=
|
|
XM_005276880.1:c.373G=
|
XP_005276937.1:p.Val125=
|
|
XM_005276881.1:c.373G=
|
XP_005276938.1:p.Val125=
|
|
XM_005276882.1:c.373G=
|
XP_005276939.1:p.Val125=
|
|
XM_005276883.1:c.373G=
|
XP_005276940.1:p.Val125=
|
|
XM_005276883.2:c.373G=
|
XP_005276940.1:p.Val125=
|
|
XM_011524889.1:c.373G=
|
XP_011523191.1:p.Val125=
|
|
XM_011524889.2:c.373G=
|
XP_011523191.1:p.Val125=
|
|
XM_011524890.1:c.373G=
|
XP_011523192.1:p.Val125=
|
|
XM_017024738.1:c.373G=
|
XP_016880227.1:p.Val125=
|
|
XM_017024739.1:c.373G=
|
XP_016880228.1:p.Val125=
|
|
XM_017024740.1:c.373G=
|
XP_016880229.1:p.Val125=
|
|
XM_017024741.1:c.373G=
|
XP_016880230.1:p.Val125=
|
