|
ENST00000411819.2:c.331-1045G=
(MSH6)
|
ENSP00000406248.2:n.331-1045G=
|
|
|
ENST00000420813.6:c.331-1045G=
(MSH6)
|
ENSP00000390382.2:n.331-1045G=
|
|
|
ENST00000455383.6:c.331-1045G=
(MSH6)
|
ENSP00000397484.2:n.331-1045G=
|
|
|
ENST00000700004.2:c.628-1045G=
(MSH6)
|
ENSP00000514752.2:n.628-1045G=
|
|
|
ENST00000699999.1:n.712-1045G=
(MSH6)
|
|
|
|
ENST00000700000.1:c.628-1045G=
(MSH6)
|
ENSP00000514749.1:n.628-1045G=
|
|
|
ENST00000700001.1:n.2202G=
(MSH6)
|
|
|
|
ENST00000700002.1:c.638-1049G=
(MSH6)
|
ENSP00000514750.1:n.638-1049G=
|
|
|
ENST00000700003.1:c.627+1503G=
(MSH6)
|
ENSP00000514751.1:n.627+1503G=
|
|
|
ENST00000234420.11:c.628-1045G=
(MSH6)
MANE Select
|
ENSP00000234420.5:n.628-1045G=
|
|
|
ENST00000540021.6:c.238-1045G=
(MSH6)
|
ENSP00000446475.1:n.238-1045G=
|
|
|
ENST00000652107.1:c.331-1045G=
(MSH6)
|
ENSP00000498629.1:n.331-1045G=
|
|
|
ENST00000673637.1:c.331-1045G=
(MSH6)
|
ENSP00000501310.1:n.331-1045G=
|
|
|
ENST00000673922.1:n.350-1045G=
(MSH6)
|
|
|
|
ENST00000234420.9:c.628-1045G=
(MSH6)
|
ENSP00000234420.4:n.628-1045G=
|
|
|
ENST00000405808.5:c.170-8126C=
(FBXO11)
|
ENSP00000385127.1:n.170-8126C=
|
|
|
ENST00000411819.1:c.331-1045G=
(MSH6)
|
ENSP00000406248.1:n.331-1045G=
|
|
|
ENST00000434234.5:c.*125-8126C=
(FBXO11)
|
ENSP00000402692.1:n.*125-8126C=
|
|
|
ENST00000445503.5:c.458-1045G=
(MSH6)
|
ENSP00000405294.1:n.458-1045G=
|
|
|
ENST00000455383.5:c.331-1045G=
(MSH6)
|
ENSP00000397484.1:n.331-1045G=
|
|
|
ENST00000456246.1:c.*116-1045G=
(MSH6)
|
ENSP00000410570.1:n.*116-1045G=
|
|
|
ENST00000538136.1:c.-275-1049G=
(MSH6)
|
ENSP00000438580.1:n.-275-1049G=
|
|
|
ENST00000540021.5:c.238-1045G=
(MSH6)
|
ENSP00000446475.1:n.238-1045G=
|
|
|
ENST00000614496.4:c.-279-1045G=
(MSH6)
|
ENSP00000477844.1:n.-279-1045G=
|
|
|
ENST00000616033.4:c.625-1045G=
(MSH6)
|
ENSP00000480261.1:n.625-1045G=
|
|
|
ENST00000622629.4:c.-2469-1045G=
(MSH6)
|
ENSP00000482078.1:n.-2469-1045G=
|
|
|
NM_000179.2:c.628-1045G= , LRG_219t1:c.628-1045G=
(MSH6)
|
NP_000170.1:n.628-1045G=
|
|
|
NM_001281492.1:c.238-1045G=
(MSH6)
|
NP_001268421.1:n.238-1045G=
|
|
|
NM_001281493.1:c.-279-1045G=
(MSH6)
|
NP_001268422.1:n.-279-1045G=
|
|
|
NM_001281494.1:c.-275-1049G=
(MSH6)
|
NP_001268423.1:n.-275-1049G=
|
|
|
XM_005264271.1:c.331-1045G=
(MSH6)
|
XP_005264328.1:n.331-1045G=
|
|
|
XM_011532798.1:c.445-1045G=
(MSH6)
|
XP_011531100.1:n.445-1045G=
|
|
|
XM_011532799.1:c.331-1045G=
(MSH6)
|
XP_011531101.1:n.331-1045G=
|
|
|
XM_011532800.1:c.331-1045G=
(MSH6)
|
XP_011531102.1:n.331-1045G=
|
|
|
XM_024452819.1:c.628-1045G=
(MSH6)
|
XP_024308587.1:n.628-1045G=
|
|
|
XM_024452820.1:c.445-1045G=
(MSH6)
|
XP_024308588.1:n.445-1045G=
|
|
|
XM_024452821.1:c.331-1045G=
(MSH6)
|
XP_024308589.1:n.331-1045G=
|
|
|
XM_024452822.1:c.-279-1045G=
(MSH6)
|
XP_024308590.1:n.-279-1045G=
|
|
|
NM_000179.3:c.628-1045G=
(MSH6)
MANE Select
|
NP_000170.1:n.628-1045G=
|
|
|
NM_001281492.2:c.238-1045G=
(MSH6)
|
NP_001268421.1:n.238-1045G=
|
|
|
NM_001281493.2:c.-279-1045G=
(MSH6)
|
NP_001268422.1:n.-279-1045G=
|
|
|
NM_001281494.2:c.-275-1049G=
(MSH6)
|
NP_001268423.1:n.-275-1049G=
|
|
