|
ENST00000411819.2:c.3520A>T
(MSH6)
|
ENSP00000406248.2:p.Asn1174Tyr
|
|
|
ENST00000420813.6:c.3520A>T
(MSH6)
|
ENSP00000390382.2:p.Asn1174Tyr
|
|
|
ENST00000455383.6:c.3520A>T
(MSH6)
|
ENSP00000397484.2:p.Asn1174Tyr
|
|
|
ENST00000700004.2:c.3433A>T
(MSH6)
|
ENSP00000514752.2:p.Asn1145Tyr
|
|
|
ENST00000699999.1:n.4491A>T
(MSH6)
|
|
|
|
ENST00000700000.1:c.2251A>T
(MSH6)
|
ENSP00000514749.1:p.Asn751Tyr
|
|
|
ENST00000700002.1:c.3823A>T
(MSH6)
|
ENSP00000514750.1:p.Asn1275Tyr
|
|
|
ENST00000700003.1:c.1272A>T
(MSH6)
|
ENSP00000514751.1:n.1272A>T
|
|
|
ENST00000700004.1:c.2590A>T
(MSH6)
|
ENSP00000514752.1:p.Asn864Tyr
|
|
|
ENST00000700005.1:n.2668A>T
(MSH6)
|
|
|
|
ENST00000700006.1:n.4975A>T
(MSH6)
|
|
|
|
ENST00000700007.1:n.2412A>T
(MSH6)
|
|
|
|
ENST00000700008.1:n.2079A>T
(MSH6)
|
|
|
|
ENST00000700009.1:n.2481A>T
(MSH6)
|
|
|
|
ENST00000700010.1:n.1226A>T
(MSH6)
|
|
|
|
ENST00000700011.1:n.3111A>T
(MSH6)
|
|
|
|
ENST00000682451.1:n.4281T>A
(FBXO11)
|
|
|
|
ENST00000684712.1:n.4543T>A
(FBXO11)
|
|
|
|
ENST00000234420.11:c.3817A>T
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Asn1273Tyr
|
|
|
ENST00000540021.6:c.3427A>T
(MSH6)
|
ENSP00000446475.1:p.Asn1143Tyr
|
|
|
ENST00000652107.1:c.3520A>T
(MSH6)
|
ENSP00000498629.1:p.Asn1174Tyr
|
|
|
ENST00000673637.1:c.3520A>T
(MSH6)
|
ENSP00000501310.1:p.Asn1174Tyr
|
|
|
ENST00000234420.9:c.3817A>T
(MSH6)
|
ENSP00000234420.4:p.Asn1273Tyr
|
|
|
ENST00000405808.5:c.169+1728T>A
(FBXO11)
|
ENSP00000385127.1:n.169+1728T>A
|
|
|
ENST00000434234.5:c.*124+1527T>A
(FBXO11)
|
ENSP00000402692.1:n.*124+1527T>A
|
|
|
ENST00000445503.5:c.*3164A>T
(MSH6)
|
ENSP00000405294.1:n.*3164A>T
|
|
|
ENST00000538136.1:c.2911A>T
(MSH6)
|
ENSP00000438580.1:p.Asn971Tyr
|
|
|
ENST00000540021.5:c.3427A>T
(MSH6)
|
ENSP00000446475.1:p.Asn1143Tyr
|
|
|
ENST00000614496.4:c.2911A>T
(MSH6)
|
ENSP00000477844.1:p.Asn971Tyr
|
|
|
ENST00000622629.4:c.718A>T
(MSH6)
|
ENSP00000482078.1:p.Asn240Tyr
|
|
|
NM_000179.2:c.3817A>T , LRG_219t1:c.3817A>T
(MSH6)
|
NP_000170.1:p.Asn1273Tyr
|
|
|
NM_001281492.1:c.3427A>T
(MSH6)
|
NP_001268421.1:p.Asn1143Tyr
|
|
|
NM_001281493.1:c.2911A>T
(MSH6)
|
NP_001268422.1:p.Asn971Tyr
|
|
|
NM_001281494.1:c.2911A>T
(MSH6)
|
NP_001268423.1:p.Asn971Tyr
|
|
|
XM_005264271.1:c.3520A>T
(MSH6)
|
XP_005264328.1:p.Asn1174Tyr
|
|
|
XM_011532798.1:c.3634A>T
(MSH6)
|
XP_011531100.1:p.Asn1212Tyr
|
|
|
XM_011532799.1:c.3520A>T
(MSH6)
|
XP_011531101.1:p.Asn1174Tyr
|
|
|
XM_011532800.1:c.3520A>T
(MSH6)
|
XP_011531102.1:p.Asn1174Tyr
|
|
|
XM_024452819.1:c.3910A>T
(MSH6)
|
XP_024308587.1:p.Asn1304Tyr
|
|
|
XM_024452820.1:c.3727A>T
(MSH6)
|
XP_024308588.1:p.Asn1243Tyr
|
|
|
XM_024452821.1:c.3613A>T
(MSH6)
|
XP_024308589.1:p.Asn1205Tyr
|
|
|
XM_024452822.1:c.3004A>T
(MSH6)
|
XP_024308590.1:p.Asn1002Tyr
|
|
|
NM_000179.3:c.3817A>T
(MSH6)
MANE Select
|
NP_000170.1:p.Asn1273Tyr
|
|
|
NM_001281492.2:c.3427A>T
(MSH6)
|
NP_001268421.1:p.Asn1143Tyr
|
|
|
NM_001281493.2:c.2911A>T
(MSH6)
|
NP_001268422.1:p.Asn971Tyr
|
|
|
NM_001281494.2:c.2911A>T
(MSH6)
|
NP_001268423.1:p.Asn971Tyr
|
|
