ENST00000411819.2:c.3523G=
(MSH6)
|
ENSP00000406248.2:p.Glu1175=
|
|
ENST00000420813.6:c.3523G=
(MSH6)
|
ENSP00000390382.2:p.Glu1175=
|
|
ENST00000455383.6:c.3523G=
(MSH6)
|
ENSP00000397484.2:p.Glu1175=
|
|
ENST00000700004.2:c.3436G=
(MSH6)
|
ENSP00000514752.2:p.Glu1146=
|
|
ENST00000699999.1:n.4494G=
(MSH6)
|
|
|
ENST00000700000.1:c.2254G=
(MSH6)
|
ENSP00000514749.1:p.Glu752=
|
|
ENST00000700002.1:c.3826G=
(MSH6)
|
ENSP00000514750.1:p.Glu1276=
|
|
ENST00000700003.1:c.1275G=
(MSH6)
|
ENSP00000514751.1:n.1275G=
|
|
ENST00000700004.1:c.2593G=
(MSH6)
|
ENSP00000514752.1:p.Glu865=
|
|
ENST00000700005.1:n.2671G=
(MSH6)
|
|
|
ENST00000700006.1:n.4978G=
(MSH6)
|
|
|
ENST00000700007.1:n.2415G=
(MSH6)
|
|
|
ENST00000700008.1:n.2082G=
(MSH6)
|
|
|
ENST00000700009.1:n.2484G=
(MSH6)
|
|
|
ENST00000700010.1:n.1229G=
(MSH6)
|
|
|
ENST00000700011.1:n.3114G=
(MSH6)
|
|
|
ENST00000682451.1:n.4278C=
(FBXO11)
|
|
|
ENST00000684712.1:n.4540C=
(FBXO11)
|
|
|
ENST00000234420.11:c.3820G=
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Glu1274=
|
|
ENST00000540021.6:c.3430G=
(MSH6)
|
ENSP00000446475.1:p.Glu1144=
|
|
ENST00000652107.1:c.3523G=
(MSH6)
|
ENSP00000498629.1:p.Glu1175=
|
|
ENST00000673637.1:c.3523G=
(MSH6)
|
ENSP00000501310.1:p.Glu1175=
|
|
ENST00000234420.9:c.3820G=
(MSH6)
|
ENSP00000234420.4:p.Glu1274=
|
|
ENST00000405808.5:c.169+1725C=
(FBXO11)
|
ENSP00000385127.1:n.169+1725C=
|
|
ENST00000434234.5:c.*124+1524C=
(FBXO11)
|
ENSP00000402692.1:n.*124+1524C=
|
|
ENST00000445503.5:c.*3167G=
(MSH6)
|
ENSP00000405294.1:n.*3167G=
|
|
ENST00000538136.1:c.2914G=
(MSH6)
|
ENSP00000438580.1:p.Glu972=
|
|
ENST00000540021.5:c.3430G=
(MSH6)
|
ENSP00000446475.1:p.Glu1144=
|
|
ENST00000614496.4:c.2914G=
(MSH6)
|
ENSP00000477844.1:p.Glu972=
|
|
ENST00000622629.4:c.721G=
(MSH6)
|
ENSP00000482078.1:p.Glu241=
|
|
NM_000179.2:c.3820G= , LRG_219t1:c.3820G=
(MSH6)
|
NP_000170.1:p.Glu1274=
|
|
NM_001281492.1:c.3430G=
(MSH6)
|
NP_001268421.1:p.Glu1144=
|
|
NM_001281493.1:c.2914G=
(MSH6)
|
NP_001268422.1:p.Glu972=
|
|
NM_001281494.1:c.2914G=
(MSH6)
|
NP_001268423.1:p.Glu972=
|
|
XM_005264271.1:c.3523G=
(MSH6)
|
XP_005264328.1:p.Glu1175=
|
|
XM_011532798.1:c.3637G=
(MSH6)
|
XP_011531100.1:p.Glu1213=
|
|
XM_011532799.1:c.3523G=
(MSH6)
|
XP_011531101.1:p.Glu1175=
|
|
XM_011532800.1:c.3523G=
(MSH6)
|
XP_011531102.1:p.Glu1175=
|
|
XM_024452819.1:c.3913G=
(MSH6)
|
XP_024308587.1:p.Glu1305=
|
|
XM_024452820.1:c.3730G=
(MSH6)
|
XP_024308588.1:p.Glu1244=
|
|
XM_024452821.1:c.3616G=
(MSH6)
|
XP_024308589.1:p.Glu1206=
|
|
XM_024452822.1:c.3007G=
(MSH6)
|
XP_024308590.1:p.Glu1003=
|
|
NM_000179.3:c.3820G=
(MSH6)
MANE Select
|
NP_000170.1:p.Glu1274=
|
|
NM_001281492.2:c.3430G=
(MSH6)
|
NP_001268421.1:p.Glu1144=
|
|
NM_001281493.2:c.2914G=
(MSH6)
|
NP_001268422.1:p.Glu972=
|
|
NM_001281494.2:c.2914G=
(MSH6)
|
NP_001268423.1:p.Glu972=
|
|