ENST00000411819.2:c.3619G>T
(MSH6)
|
ENSP00000406248.2:p.Ala1207Ser
|
|
ENST00000420813.6:c.3619G>T
(MSH6)
|
ENSP00000390382.2:p.Ala1207Ser
|
|
ENST00000455383.6:c.3619G>T
(MSH6)
|
ENSP00000397484.2:p.Ala1207Ser
|
|
ENST00000700004.2:c.3532G>T
(MSH6)
|
ENSP00000514752.2:p.Ala1178Ser
|
|
ENST00000699999.1:n.4590G>T
(MSH6)
|
|
|
ENST00000700000.1:c.2350G>T
(MSH6)
|
ENSP00000514749.1:p.Ala784Ser
|
|
ENST00000700002.1:c.3922G>T
(MSH6)
|
ENSP00000514750.1:p.Ala1308Ser
|
|
ENST00000700003.1:c.1371G>T
(MSH6)
|
ENSP00000514751.1:n.1371G>T
|
|
ENST00000700004.1:c.2689G>T
(MSH6)
|
ENSP00000514752.1:p.Ala897Ser
|
|
ENST00000700005.1:n.2767G>T
(MSH6)
|
|
|
ENST00000700006.1:n.5074G>T
(MSH6)
|
|
|
ENST00000700007.1:n.2511G>T
(MSH6)
|
|
|
ENST00000700008.1:n.2178G>T
(MSH6)
|
|
|
ENST00000700009.1:n.2580G>T
(MSH6)
|
|
|
ENST00000700010.1:n.1325G>T
(MSH6)
|
|
|
ENST00000700011.1:n.3210G>T
(MSH6)
|
|
|
ENST00000682451.1:n.4182C>A
(FBXO11)
|
|
|
ENST00000684712.1:n.4444C>A
(FBXO11)
|
|
|
ENST00000234420.11:c.3916G>T
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Ala1306Ser
|
|
ENST00000540021.6:c.3526G>T
(MSH6)
|
ENSP00000446475.1:p.Ala1176Ser
|
|
ENST00000652107.1:c.3619G>T
(MSH6)
|
ENSP00000498629.1:p.Ala1207Ser
|
|
ENST00000673637.1:c.3619G>T
(MSH6)
|
ENSP00000501310.1:p.Ala1207Ser
|
|
ENST00000234420.9:c.3916G>T
(MSH6)
|
ENSP00000234420.4:p.Ala1306Ser
|
|
ENST00000405808.5:c.169+1629C>A
(FBXO11)
|
ENSP00000385127.1:n.169+1629C>A
|
|
ENST00000434234.5:c.*124+1428C>A
(FBXO11)
|
ENSP00000402692.1:n.*124+1428C>A
|
|
ENST00000445503.5:c.*3263G>T
(MSH6)
|
ENSP00000405294.1:n.*3263G>T
|
|
ENST00000538136.1:c.3010G>T
(MSH6)
|
ENSP00000438580.1:p.Ala1004Ser
|
|
ENST00000540021.5:c.3526G>T
(MSH6)
|
ENSP00000446475.1:p.Ala1176Ser
|
|
ENST00000614496.4:c.3010G>T
(MSH6)
|
ENSP00000477844.1:p.Ala1004Ser
|
|
ENST00000622629.4:c.817G>T
(MSH6)
|
ENSP00000482078.1:p.Ala273Ser
|
|
NM_000179.2:c.3916G>T , LRG_219t1:c.3916G>T
(MSH6)
|
NP_000170.1:p.Ala1306Ser
|
|
NM_001281492.1:c.3526G>T
(MSH6)
|
NP_001268421.1:p.Ala1176Ser
|
|
NM_001281493.1:c.3010G>T
(MSH6)
|
NP_001268422.1:p.Ala1004Ser
|
|
NM_001281494.1:c.3010G>T
(MSH6)
|
NP_001268423.1:p.Ala1004Ser
|
|
XM_005264271.1:c.3619G>T
(MSH6)
|
XP_005264328.1:p.Ala1207Ser
|
|
XM_011532798.1:c.3733G>T
(MSH6)
|
XP_011531100.1:p.Ala1245Ser
|
|
XM_011532799.1:c.3619G>T
(MSH6)
|
XP_011531101.1:p.Ala1207Ser
|
|
XM_011532800.1:c.3619G>T
(MSH6)
|
XP_011531102.1:p.Ala1207Ser
|
|
XM_024452819.1:c.4009G>T
(MSH6)
|
XP_024308587.1:p.Ala1337Ser
|
|
XM_024452820.1:c.3826G>T
(MSH6)
|
XP_024308588.1:p.Ala1276Ser
|
|
XM_024452821.1:c.3712G>T
(MSH6)
|
XP_024308589.1:p.Ala1238Ser
|
|
XM_024452822.1:c.3103G>T
(MSH6)
|
XP_024308590.1:p.Ala1035Ser
|
|
NM_000179.3:c.3916G>T
(MSH6)
MANE Select
|
NP_000170.1:p.Ala1306Ser
|
|
NM_001281492.2:c.3526G>T
(MSH6)
|
NP_001268421.1:p.Ala1176Ser
|
|
NM_001281493.2:c.3010G>T
(MSH6)
|
NP_001268422.1:p.Ala1004Ser
|
|
NM_001281494.2:c.3010G>T
(MSH6)
|
NP_001268423.1:p.Ala1004Ser
|
|