ENST00000561667.2:c.*96G=
|
ENSP00000512522.1:n.*96G=
|
|
ENST00000564475.6:c.1906G=
|
ENSP00000454977.2:p.Ala636=
|
|
ENST00000567205.2:c.1906G=
|
ENSP00000457027.2:p.Ala636=
|
|
ENST00000567284.7:n.1949G=
|
|
|
ENST00000567510.2:c.402G=
|
ENSP00000455969.1:n.402G=
|
|
ENST00000568369.6:c.1906G=
|
ENSP00000456829.1:p.Ala636=
|
|
ENST00000696274.1:n.1867G=
|
|
|
ENST00000696275.1:c.*1141G=
|
ENSP00000512517.1:n.*1141G=
|
|
ENST00000696276.1:n.1949G=
|
|
|
ENST00000696286.1:c.1906G=
|
ENSP00000512523.1:p.Ala636=
|
|
ENST00000696287.1:c.1906G=
|
ENSP00000512524.1:p.Ala636=
|
|
ENST00000696291.1:c.*1322G=
|
ENSP00000512530.1:n.*1322G=
|
|
ENST00000389301.8:c.1906G=
MANE Select
|
ENSP00000373952.3:p.Ala636=
|
|
ENST00000389301.7:c.1906G=
|
ENSP00000373952.3:p.Ala636=
|
|
ENST00000567284.6:n.130G=
|
|
|
ENST00000567510.1:c.402G=
|
ENSP00000455969.1:n.402G=
|
|
ENST00000568369.5:c.1906G=
|
ENSP00000456829.1:p.Ala636=
|
|
NM_000135.2:c.1906G= , LRG_495t1:c.1906G=
|
NP_000126.2:p.Ala636=
|
|
NM_001286167.1:c.1906G=
|
NP_001273096.1:p.Ala636=
|
|
XM_005256294.3:c.1906G=
|
XP_005256351.1:p.Ala636=
|
|
XM_011522945.1:c.1906G=
|
XP_011521247.1:p.Ala636=
|
|
XM_011522946.1:c.883G=
|
XP_011521248.1:p.Ala295=
|
|
XM_011522947.1:c.883G=
|
XP_011521249.1:p.Ala295=
|
|
XM_011522948.1:c.1906G=
|
XP_011521250.1:p.Ala636=
|
|
XR_933244.1:n.1949G=
|
|
|
XR_933245.1:n.1949G=
|
|
|
XR_933246.1:n.1949G=
|
|
|
XR_933247.1:n.1949G=
|
|
|
NM_000135.3:c.1906G=
|
NP_000126.2:p.Ala636=
|
|
NM_001286167.2:c.1906G=
|
NP_001273096.1:p.Ala636=
|
|
XM_005256294.4:c.1906G=
|
XP_005256351.1:p.Ala636=
|
|
XM_011522945.2:c.1906G=
|
XP_011521247.1:p.Ala636=
|
|
XM_011522946.3:c.883G=
|
XP_011521248.1:p.Ala295=
|
|
XM_011522947.2:c.883G=
|
XP_011521249.1:p.Ala295=
|
|
XM_011522948.2:c.1906G=
|
XP_011521250.1:p.Ala636=
|
|
XM_017023044.2:c.1906G=
|
XP_016878533.1:p.Ala636=
|
|
XM_017023045.1:c.1906G=
|
XP_016878534.1:p.Ala636=
|
|
XM_024450189.1:c.883G=
|
XP_024305957.1:p.Ala295=
|
|
XR_001751866.1:n.1949G=
|
|
|
XR_933244.2:n.1949G=
|
|
|
XR_933245.2:n.1949G=
|
|
|
XR_933247.2:n.1949G=
|
|
|
NM_000135.4:c.1906G=
MANE Select
|
NP_000126.2:p.Ala636=
|
|
NM_001286167.3:c.1906G=
|
NP_001273096.1:p.Ala636=
|
|