ENST00000411819.2:c.1670C=
(MSH6)
|
ENSP00000406248.2:p.Pro557=
|
|
ENST00000420813.6:c.1670C=
(MSH6)
|
ENSP00000390382.2:p.Pro557=
|
|
ENST00000455383.6:c.1670C=
(MSH6)
|
ENSP00000397484.2:p.Pro557=
|
|
ENST00000700004.2:c.1967C=
(MSH6)
|
ENSP00000514752.2:p.Pro656=
|
|
ENST00000699999.1:n.2051C=
(MSH6)
|
|
|
ENST00000700000.1:c.1606+361C=
(MSH6)
|
ENSP00000514749.1:n.1606+361C=
|
|
ENST00000700002.1:c.1973C=
(MSH6)
|
ENSP00000514750.1:p.Pro658=
|
|
ENST00000700003.1:c.628-3470C=
(MSH6)
|
ENSP00000514751.1:n.628-3470C=
|
|
ENST00000700004.1:c.1124C=
(MSH6)
|
ENSP00000514752.1:p.Pro375=
|
|
ENST00000234420.11:c.1967C=
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Pro656=
|
|
ENST00000540021.6:c.1577C=
(MSH6)
|
ENSP00000446475.1:p.Pro526=
|
|
ENST00000652107.1:c.1670C=
(MSH6)
|
ENSP00000498629.1:p.Pro557=
|
|
ENST00000673637.1:c.1670C=
(MSH6)
|
ENSP00000501310.1:p.Pro557=
|
|
ENST00000234420.9:c.1967C=
(MSH6)
|
ENSP00000234420.4:p.Pro656=
|
|
ENST00000405808.5:c.169+8245G=
(FBXO11)
|
ENSP00000385127.1:n.169+8245G=
|
|
ENST00000434234.5:c.*124+8044G=
(FBXO11)
|
ENSP00000402692.1:n.*124+8044G=
|
|
ENST00000445503.5:c.*1314C=
(MSH6)
|
ENSP00000405294.1:n.*1314C=
|
|
ENST00000538136.1:c.1061C=
(MSH6)
|
ENSP00000438580.1:p.Pro354=
|
|
ENST00000540021.5:c.1577C=
(MSH6)
|
ENSP00000446475.1:p.Pro526=
|
|
ENST00000614496.4:c.1061C=
(MSH6)
|
ENSP00000477844.1:p.Pro354=
|
|
ENST00000616033.4:c.1964C=
(MSH6)
|
ENSP00000480261.1:p.Pro655=
|
|
ENST00000622629.4:c.-1130C=
(MSH6)
|
ENSP00000482078.1:n.-1130C=
|
|
NM_000179.2:c.1967C= , LRG_219t1:c.1967C=
(MSH6)
|
NP_000170.1:p.Pro656=
|
|
NM_001281492.1:c.1577C=
(MSH6)
|
NP_001268421.1:p.Pro526=
|
|
NM_001281493.1:c.1061C=
(MSH6)
|
NP_001268422.1:p.Pro354=
|
|
NM_001281494.1:c.1061C=
(MSH6)
|
NP_001268423.1:p.Pro354=
|
|
XM_005264271.1:c.1670C=
(MSH6)
|
XP_005264328.1:p.Pro557=
|
|
XM_011532798.1:c.1784C=
(MSH6)
|
XP_011531100.1:p.Pro595=
|
|
XM_011532799.1:c.1670C=
(MSH6)
|
XP_011531101.1:p.Pro557=
|
|
XM_011532800.1:c.1670C=
(MSH6)
|
XP_011531102.1:p.Pro557=
|
|
XM_024452819.1:c.1967C=
(MSH6)
|
XP_024308587.1:p.Pro656=
|
|
XM_024452820.1:c.1784C=
(MSH6)
|
XP_024308588.1:p.Pro595=
|
|
XM_024452821.1:c.1670C=
(MSH6)
|
XP_024308589.1:p.Pro557=
|
|
XM_024452822.1:c.1061C=
(MSH6)
|
XP_024308590.1:p.Pro354=
|
|
NM_000179.3:c.1967C=
(MSH6)
MANE Select
|
NP_000170.1:p.Pro656=
|
|
NM_001281492.2:c.1577C=
(MSH6)
|
NP_001268421.1:p.Pro526=
|
|
NM_001281493.2:c.1061C=
(MSH6)
|
NP_001268422.1:p.Pro354=
|
|
NM_001281494.2:c.1061C=
(MSH6)
|
NP_001268423.1:p.Pro354=
|
|