|
ENST00000411819.2:c.3518A>T
(MSH6)
|
ENSP00000406248.2:p.Glu1173Val
|
|
|
ENST00000420813.6:c.3518A>T
(MSH6)
|
ENSP00000390382.2:p.Glu1173Val
|
|
|
ENST00000455383.6:c.3518A>T
(MSH6)
|
ENSP00000397484.2:p.Glu1173Val
|
|
|
ENST00000700004.2:c.3431A>T
(MSH6)
|
ENSP00000514752.2:p.Glu1144Val
|
|
|
ENST00000699999.1:n.4489A>T
(MSH6)
|
|
|
|
ENST00000700000.1:c.2249A>T
(MSH6)
|
ENSP00000514749.1:p.Glu750Val
|
|
|
ENST00000700002.1:c.3821A>T
(MSH6)
|
ENSP00000514750.1:p.Glu1274Val
|
|
|
ENST00000700003.1:c.1270A>T
(MSH6)
|
ENSP00000514751.1:n.1270A>T
|
|
|
ENST00000700004.1:c.2588A>T
(MSH6)
|
ENSP00000514752.1:p.Glu863Val
|
|
|
ENST00000700005.1:n.2666A>T
(MSH6)
|
|
|
|
ENST00000700006.1:n.4973A>T
(MSH6)
|
|
|
|
ENST00000700007.1:n.2410A>T
(MSH6)
|
|
|
|
ENST00000700008.1:n.2077A>T
(MSH6)
|
|
|
|
ENST00000700009.1:n.2479A>T
(MSH6)
|
|
|
|
ENST00000700010.1:n.1224A>T
(MSH6)
|
|
|
|
ENST00000700011.1:n.3109A>T
(MSH6)
|
|
|
|
ENST00000682451.1:n.4283T>A
(FBXO11)
|
|
|
|
ENST00000684712.1:n.4545T>A
(FBXO11)
|
|
|
|
ENST00000234420.11:c.3815A>T
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Glu1272Val
|
|
|
ENST00000540021.6:c.3425A>T
(MSH6)
|
ENSP00000446475.1:p.Glu1142Val
|
|
|
ENST00000652107.1:c.3518A>T
(MSH6)
|
ENSP00000498629.1:p.Glu1173Val
|
|
|
ENST00000673637.1:c.3518A>T
(MSH6)
|
ENSP00000501310.1:p.Glu1173Val
|
|
|
ENST00000234420.9:c.3815A>T
(MSH6)
|
ENSP00000234420.4:p.Glu1272Val
|
|
|
ENST00000405808.5:c.169+1730T>A
(FBXO11)
|
ENSP00000385127.1:n.169+1730T>A
|
|
|
ENST00000434234.5:c.*124+1529T>A
(FBXO11)
|
ENSP00000402692.1:n.*124+1529T>A
|
|
|
ENST00000445503.5:c.*3162A>T
(MSH6)
|
ENSP00000405294.1:n.*3162A>T
|
|
|
ENST00000538136.1:c.2909A>T
(MSH6)
|
ENSP00000438580.1:p.Glu970Val
|
|
|
ENST00000540021.5:c.3425A>T
(MSH6)
|
ENSP00000446475.1:p.Glu1142Val
|
|
|
ENST00000614496.4:c.2909A>T
(MSH6)
|
ENSP00000477844.1:p.Glu970Val
|
|
|
ENST00000622629.4:c.716A>T
(MSH6)
|
ENSP00000482078.1:p.Glu239Val
|
|
|
NM_000179.2:c.3815A>T , LRG_219t1:c.3815A>T
(MSH6)
|
NP_000170.1:p.Glu1272Val
|
|
|
NM_001281492.1:c.3425A>T
(MSH6)
|
NP_001268421.1:p.Glu1142Val
|
|
|
NM_001281493.1:c.2909A>T
(MSH6)
|
NP_001268422.1:p.Glu970Val
|
|
|
NM_001281494.1:c.2909A>T
(MSH6)
|
NP_001268423.1:p.Glu970Val
|
|
|
XM_005264271.1:c.3518A>T
(MSH6)
|
XP_005264328.1:p.Glu1173Val
|
|
|
XM_011532798.1:c.3632A>T
(MSH6)
|
XP_011531100.1:p.Glu1211Val
|
|
|
XM_011532799.1:c.3518A>T
(MSH6)
|
XP_011531101.1:p.Glu1173Val
|
|
|
XM_011532800.1:c.3518A>T
(MSH6)
|
XP_011531102.1:p.Glu1173Val
|
|
|
XM_024452819.1:c.3908A>T
(MSH6)
|
XP_024308587.1:p.Glu1303Val
|
|
|
XM_024452820.1:c.3725A>T
(MSH6)
|
XP_024308588.1:p.Glu1242Val
|
|
|
XM_024452821.1:c.3611A>T
(MSH6)
|
XP_024308589.1:p.Glu1204Val
|
|
|
XM_024452822.1:c.3002A>T
(MSH6)
|
XP_024308590.1:p.Glu1001Val
|
|
|
NM_000179.3:c.3815A>T
(MSH6)
MANE Select
|
NP_000170.1:p.Glu1272Val
|
|
|
NM_001281492.2:c.3425A>T
(MSH6)
|
NP_001268421.1:p.Glu1142Val
|
|
|
NM_001281493.2:c.2909A>T
(MSH6)
|
NP_001268422.1:p.Glu970Val
|
|
|
NM_001281494.2:c.2909A>T
(MSH6)
|
NP_001268423.1:p.Glu970Val
|
|
