ENST00000411819.2:c.3549T>G
(MSH6)
|
ENSP00000406248.2:p.Thr1183=
|
|
ENST00000420813.6:c.3549T>G
(MSH6)
|
ENSP00000390382.2:p.Thr1183=
|
|
ENST00000455383.6:c.3549T>G
(MSH6)
|
ENSP00000397484.2:p.Thr1183=
|
|
ENST00000700004.2:c.3462T>G
(MSH6)
|
ENSP00000514752.2:p.Thr1154=
|
|
ENST00000699999.1:n.4520T>G
(MSH6)
|
|
|
ENST00000700000.1:c.2280T>G
(MSH6)
|
ENSP00000514749.1:p.Thr760=
|
|
ENST00000700002.1:c.3852T>G
(MSH6)
|
ENSP00000514750.1:p.Thr1284=
|
|
ENST00000700003.1:c.1301T>G
(MSH6)
|
ENSP00000514751.1:n.1301T>G
|
|
ENST00000700004.1:c.2619T>G
(MSH6)
|
ENSP00000514752.1:p.Thr873=
|
|
ENST00000700005.1:n.2697T>G
(MSH6)
|
|
|
ENST00000700006.1:n.5004T>G
(MSH6)
|
|
|
ENST00000700007.1:n.2441T>G
(MSH6)
|
|
|
ENST00000700008.1:n.2108T>G
(MSH6)
|
|
|
ENST00000700009.1:n.2510T>G
(MSH6)
|
|
|
ENST00000700010.1:n.1255T>G
(MSH6)
|
|
|
ENST00000700011.1:n.3140T>G
(MSH6)
|
|
|
ENST00000682451.1:n.4252A>C
(FBXO11)
|
|
|
ENST00000684712.1:n.4514A>C
(FBXO11)
|
|
|
ENST00000234420.11:c.3846T>G
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Thr1282=
|
|
ENST00000540021.6:c.3456T>G
(MSH6)
|
ENSP00000446475.1:p.Thr1152=
|
|
ENST00000652107.1:c.3549T>G
(MSH6)
|
ENSP00000498629.1:p.Thr1183=
|
|
ENST00000673637.1:c.3549T>G
(MSH6)
|
ENSP00000501310.1:p.Thr1183=
|
|
ENST00000234420.9:c.3846T>G
(MSH6)
|
ENSP00000234420.4:p.Thr1282=
|
|
ENST00000405808.5:c.169+1699A>C
(FBXO11)
|
ENSP00000385127.1:n.169+1699A>C
|
|
ENST00000434234.5:c.*124+1498A>C
(FBXO11)
|
ENSP00000402692.1:n.*124+1498A>C
|
|
ENST00000445503.5:c.*3193T>G
(MSH6)
|
ENSP00000405294.1:n.*3193T>G
|
|
ENST00000538136.1:c.2940T>G
(MSH6)
|
ENSP00000438580.1:p.Thr980=
|
|
ENST00000540021.5:c.3456T>G
(MSH6)
|
ENSP00000446475.1:p.Thr1152=
|
|
ENST00000614496.4:c.2940T>G
(MSH6)
|
ENSP00000477844.1:p.Thr980=
|
|
ENST00000622629.4:c.747T>G
(MSH6)
|
ENSP00000482078.1:p.Thr249=
|
|
NM_000179.2:c.3846T>G , LRG_219t1:c.3846T>G
(MSH6)
|
NP_000170.1:p.Thr1282=
|
|
NM_001281492.1:c.3456T>G
(MSH6)
|
NP_001268421.1:p.Thr1152=
|
|
NM_001281493.1:c.2940T>G
(MSH6)
|
NP_001268422.1:p.Thr980=
|
|
NM_001281494.1:c.2940T>G
(MSH6)
|
NP_001268423.1:p.Thr980=
|
|
XM_005264271.1:c.3549T>G
(MSH6)
|
XP_005264328.1:p.Thr1183=
|
|
XM_011532798.1:c.3663T>G
(MSH6)
|
XP_011531100.1:p.Thr1221=
|
|
XM_011532799.1:c.3549T>G
(MSH6)
|
XP_011531101.1:p.Thr1183=
|
|
XM_011532800.1:c.3549T>G
(MSH6)
|
XP_011531102.1:p.Thr1183=
|
|
XM_024452819.1:c.3939T>G
(MSH6)
|
XP_024308587.1:p.Thr1313=
|
|
XM_024452820.1:c.3756T>G
(MSH6)
|
XP_024308588.1:p.Thr1252=
|
|
XM_024452821.1:c.3642T>G
(MSH6)
|
XP_024308589.1:p.Thr1214=
|
|
XM_024452822.1:c.3033T>G
(MSH6)
|
XP_024308590.1:p.Thr1011=
|
|
NM_000179.3:c.3846T>G
(MSH6)
MANE Select
|
NP_000170.1:p.Thr1282=
|
|
NM_001281492.2:c.3456T>G
(MSH6)
|
NP_001268421.1:p.Thr1152=
|
|
NM_001281493.2:c.2940T>G
(MSH6)
|
NP_001268422.1:p.Thr980=
|
|
NM_001281494.2:c.2940T>G
(MSH6)
|
NP_001268423.1:p.Thr980=
|
|