|
ENST00000411819.2:c.534A>T
(MSH6)
|
ENSP00000406248.2:p.Glu178Asp
|
|
|
ENST00000420813.6:c.534A>T
(MSH6)
|
ENSP00000390382.2:p.Glu178Asp
|
|
|
ENST00000455383.6:c.534A>T
(MSH6)
|
ENSP00000397484.2:p.Glu178Asp
|
|
|
ENST00000700004.2:c.831A>T
(MSH6)
|
ENSP00000514752.2:p.Glu277Asp
|
|
|
ENST00000699999.1:n.915A>T
(MSH6)
|
|
|
|
ENST00000700000.1:c.831A>T
(MSH6)
|
ENSP00000514749.1:p.Glu277Asp
|
|
|
ENST00000700002.1:c.837A>T
(MSH6)
|
ENSP00000514750.1:p.Glu279Asp
|
|
|
ENST00000700003.1:c.627+2751A>T
(MSH6)
|
ENSP00000514751.1:n.627+2751A>T
|
|
|
ENST00000234420.11:c.831A>T
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Glu277Asp
|
|
|
ENST00000540021.6:c.441A>T
(MSH6)
|
ENSP00000446475.1:p.Glu147Asp
|
|
|
ENST00000652107.1:c.534A>T
(MSH6)
|
ENSP00000498629.1:p.Glu178Asp
|
|
|
ENST00000673637.1:c.534A>T
(MSH6)
|
ENSP00000501310.1:p.Glu178Asp
|
|
|
ENST00000673922.1:n.553A>T
(MSH6)
|
|
|
|
ENST00000234420.9:c.831A>T
(MSH6)
|
ENSP00000234420.4:p.Glu277Asp
|
|
|
ENST00000405808.5:c.170-9374T>A
(FBXO11)
|
ENSP00000385127.1:n.170-9374T>A
|
|
|
ENST00000434234.5:c.*124+9180T>A
(FBXO11)
|
ENSP00000402692.1:n.*124+9180T>A
|
|
|
ENST00000445503.5:c.*178A>T
(MSH6)
|
ENSP00000405294.1:n.*178A>T
|
|
|
ENST00000456246.1:c.*319A>T
(MSH6)
|
ENSP00000410570.1:n.*319A>T
|
|
|
ENST00000538136.1:c.-76A>T
(MSH6)
|
ENSP00000438580.1:n.-76A>T
|
|
|
ENST00000540021.5:c.441A>T
(MSH6)
|
ENSP00000446475.1:p.Glu147Asp
|
|
|
ENST00000614496.4:c.-76A>T
(MSH6)
|
ENSP00000477844.1:n.-76A>T
|
|
|
ENST00000616033.4:c.828A>T
(MSH6)
|
ENSP00000480261.1:p.Glu276Asp
|
|
|
ENST00000622629.4:c.-2266A>T
(MSH6)
|
ENSP00000482078.1:n.-2266A>T
|
|
|
NM_000179.2:c.831A>T , LRG_219t1:c.831A>T
(MSH6)
|
NP_000170.1:p.Glu277Asp
|
|
|
NM_001281492.1:c.441A>T
(MSH6)
|
NP_001268421.1:p.Glu147Asp
|
|
|
NM_001281493.1:c.-76A>T
(MSH6)
|
NP_001268422.1:n.-76A>T
|
|
|
NM_001281494.1:c.-76A>T
(MSH6)
|
NP_001268423.1:n.-76A>T
|
|
|
XM_005264271.1:c.534A>T
(MSH6)
|
XP_005264328.1:p.Glu178Asp
|
|
|
XM_011532798.1:c.648A>T
(MSH6)
|
XP_011531100.1:p.Glu216Asp
|
|
|
XM_011532799.1:c.534A>T
(MSH6)
|
XP_011531101.1:p.Glu178Asp
|
|
|
XM_011532800.1:c.534A>T
(MSH6)
|
XP_011531102.1:p.Glu178Asp
|
|
|
XM_024452819.1:c.831A>T
(MSH6)
|
XP_024308587.1:p.Glu277Asp
|
|
|
XM_024452820.1:c.648A>T
(MSH6)
|
XP_024308588.1:p.Glu216Asp
|
|
|
XM_024452821.1:c.534A>T
(MSH6)
|
XP_024308589.1:p.Glu178Asp
|
|
|
XM_024452822.1:c.-76A>T
(MSH6)
|
XP_024308590.1:n.-76A>T
|
|
|
NM_000179.3:c.831A>T
(MSH6)
MANE Select
|
NP_000170.1:p.Glu277Asp
|
|
|
NM_001281492.2:c.441A>T
(MSH6)
|
NP_001268421.1:p.Glu147Asp
|
|
|
NM_001281493.2:c.-76A>T
(MSH6)
|
NP_001268422.1:n.-76A>T
|
|
|
NM_001281494.2:c.-76A>T
(MSH6)
|
NP_001268423.1:n.-76A>T
|
|
