|
ENST00000411819.2:c.3315A>T
(MSH6)
|
ENSP00000406248.2:p.Ala1105=
|
|
|
ENST00000420813.6:c.3315A>T
(MSH6)
|
ENSP00000390382.2:p.Ala1105=
|
|
|
ENST00000455383.6:c.3315A>T
(MSH6)
|
ENSP00000397484.2:p.Ala1105=
|
|
|
ENST00000700004.2:c.3228A>T
(MSH6)
|
ENSP00000514752.2:p.Ala1076=
|
|
|
ENST00000699999.1:n.4286A>T
(MSH6)
|
|
|
|
ENST00000700000.1:c.2046A>T
(MSH6)
|
ENSP00000514749.1:p.Ala682=
|
|
|
ENST00000700002.1:c.3618A>T
(MSH6)
|
ENSP00000514750.1:p.Ala1206=
|
|
|
ENST00000700003.1:c.1067A>T
(MSH6)
|
ENSP00000514751.1:n.1067A>T
|
|
|
ENST00000700004.1:c.2385A>T
(MSH6)
|
ENSP00000514752.1:p.Ala795=
|
|
|
ENST00000700005.1:n.2463A>T
(MSH6)
|
|
|
|
ENST00000700006.1:n.4274A>T
(MSH6)
|
|
|
|
ENST00000700007.1:n.2207A>T
(MSH6)
|
|
|
|
ENST00000700008.1:n.1781A>T
(MSH6)
|
|
|
|
ENST00000700009.1:n.1780A>T
(MSH6)
|
|
|
|
ENST00000700010.1:n.1021A>T
(MSH6)
|
|
|
|
ENST00000700011.1:n.2906A>T
(MSH6)
|
|
|
|
ENST00000234420.11:c.3612A>T
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Ala1204=
|
|
|
ENST00000540021.6:c.3222A>T
(MSH6)
|
ENSP00000446475.1:p.Ala1074=
|
|
|
ENST00000652107.1:c.3315A>T
(MSH6)
|
ENSP00000498629.1:p.Ala1105=
|
|
|
ENST00000673637.1:c.3315A>T
(MSH6)
|
ENSP00000501310.1:p.Ala1105=
|
|
|
ENST00000234420.9:c.3612A>T
(MSH6)
|
ENSP00000234420.4:p.Ala1204=
|
|
|
ENST00000405808.5:c.169+2522T>A
(FBXO11)
|
ENSP00000385127.1:n.169+2522T>A
|
|
|
ENST00000434234.5:c.*124+2321T>A
(FBXO11)
|
ENSP00000402692.1:n.*124+2321T>A
|
|
|
ENST00000445503.5:c.*2959A>T
(MSH6)
|
ENSP00000405294.1:n.*2959A>T
|
|
|
ENST00000538136.1:c.2706A>T
(MSH6)
|
ENSP00000438580.1:p.Ala902=
|
|
|
ENST00000540021.5:c.3222A>T
(MSH6)
|
ENSP00000446475.1:p.Ala1074=
|
|
|
ENST00000614496.4:c.2706A>T
(MSH6)
|
ENSP00000477844.1:p.Ala902=
|
|
|
ENST00000622629.4:c.516A>T
(MSH6)
|
ENSP00000482078.1:p.Ala172=
|
|
|
NM_000179.2:c.3612A>T , LRG_219t1:c.3612A>T
(MSH6)
|
NP_000170.1:p.Ala1204=
|
|
|
NM_001281492.1:c.3222A>T
(MSH6)
|
NP_001268421.1:p.Ala1074=
|
|
|
NM_001281493.1:c.2706A>T
(MSH6)
|
NP_001268422.1:p.Ala902=
|
|
|
NM_001281494.1:c.2706A>T
(MSH6)
|
NP_001268423.1:p.Ala902=
|
|
|
XM_005264271.1:c.3315A>T
(MSH6)
|
XP_005264328.1:p.Ala1105=
|
|
|
XM_011532798.1:c.3429A>T
(MSH6)
|
XP_011531100.1:p.Ala1143=
|
|
|
XM_011532799.1:c.3315A>T
(MSH6)
|
XP_011531101.1:p.Ala1105=
|
|
|
XM_011532800.1:c.3315A>T
(MSH6)
|
XP_011531102.1:p.Ala1105=
|
|
|
XM_024452819.1:c.3612A>T
(MSH6)
|
XP_024308587.1:p.Ala1204=
|
|
|
XM_024452820.1:c.3429A>T
(MSH6)
|
XP_024308588.1:p.Ala1143=
|
|
|
XM_024452821.1:c.3315A>T
(MSH6)
|
XP_024308589.1:p.Ala1105=
|
|
|
XM_024452822.1:c.2706A>T
(MSH6)
|
XP_024308590.1:p.Ala902=
|
|
|
NM_000179.3:c.3612A>T
(MSH6)
MANE Select
|
NP_000170.1:p.Ala1204=
|
|
|
NM_001281492.2:c.3222A>T
(MSH6)
|
NP_001268421.1:p.Ala1074=
|
|
|
NM_001281493.2:c.2706A>T
(MSH6)
|
NP_001268422.1:p.Ala902=
|
|
|
NM_001281494.2:c.2706A>T
(MSH6)
|
NP_001268423.1:p.Ala902=
|
|
