ENST00000411819.2:c.3549_3570delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000406248.2:p.Thr1183=
|
|
ENST00000420813.6:c.3549_3570delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000390382.2:p.Thr1183=
|
|
ENST00000455383.6:c.3549_3570delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000397484.2:p.Thr1183=
|
|
ENST00000700004.2:c.3462_3483delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000514752.2:p.Thr1154=
|
|
ENST00000699999.1:n.4520_4541delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
|
|
ENST00000700000.1:c.2280_2301delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000514749.1:p.Thr760=
|
|
ENST00000700002.1:c.3852_3873delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000514750.1:p.Thr1284=
|
|
ENST00000700003.1:c.1301_1322delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000514751.1:n.1301_1322delinsTATTACGTTCCTCTATAAATTC
|
|
ENST00000700004.1:c.2619_2640delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000514752.1:p.Thr873=
|
|
ENST00000700005.1:n.2697_2718delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
|
|
ENST00000700006.1:n.5004_5025delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
|
|
ENST00000700007.1:n.2441_2462delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
|
|
ENST00000700008.1:n.2108_2129delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
|
|
ENST00000700009.1:n.2510_2531delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
|
|
ENST00000700010.1:n.1255_1276delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
|
|
ENST00000700011.1:n.3140_3161delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
|
|
ENST00000682451.1:n.4231_4252delinsGAATTTATAGAGGAACGTAATA
(FBXO11)
|
|
|
ENST00000684712.1:n.4493_4514delinsGAATTTATAGAGGAACGTAATA
(FBXO11)
|
|
|
ENST00000234420.11:c.3846_3867delinsTATTACGTTCCTCTATAAATTC
(MSH6)
MANE Select
|
ENSP00000234420.5:p.Thr1282=
|
|
ENST00000540021.6:c.3456_3477delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000446475.1:p.Thr1152=
|
|
ENST00000652107.1:c.3549_3570delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000498629.1:p.Thr1183=
|
|
ENST00000673637.1:c.3549_3570delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000501310.1:p.Thr1183=
|
|
ENST00000234420.9:c.3846_3867delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000234420.4:p.Thr1282=
|
|
ENST00000405808.5:c.169+1678_169+1699delinsGAATTTATAGAGGAACGTAATA
(FBXO11)
|
ENSP00000385127.1:n.169+1678_169+1699delinsGAATTTATAGAGGAACGT...
|
|
ENST00000434234.5:c.*124+1477_*124+1498delinsGAATTTATAGAGGAACGTAATA
(FBXO11)
|
ENSP00000402692.1:n.*124+1477_*124+1498delinsGAATTTATAGAGGAAC...
|
|
ENST00000445503.5:c.*3193_*3214delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000405294.1:n.*3193_*3214delinsTATTACGTTCCTCTATAAATTC
|
|
ENST00000538136.1:c.2940_2961delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000438580.1:p.Thr980=
|
|
ENST00000540021.5:c.3456_3477delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000446475.1:p.Thr1152=
|
|
ENST00000614496.4:c.2940_2961delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000477844.1:p.Thr980=
|
|
ENST00000622629.4:c.747_768delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
ENSP00000482078.1:p.Thr249=
|
|
NM_000179.2:c.3846_3867delinsTATTACGTTCCTCTATAAATTC , LRG_219t1:c.3846_3867delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
NP_000170.1:p.Thr1282=
|
|
NM_001281492.1:c.3456_3477delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
NP_001268421.1:p.Thr1152=
|
|
NM_001281493.1:c.2940_2961delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
NP_001268422.1:p.Thr980=
|
|
NM_001281494.1:c.2940_2961delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
NP_001268423.1:p.Thr980=
|
|
XM_005264271.1:c.3549_3570delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
XP_005264328.1:p.Thr1183=
|
|
XM_011532798.1:c.3663_3684delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
XP_011531100.1:p.Thr1221=
|
|
XM_011532799.1:c.3549_3570delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
XP_011531101.1:p.Thr1183=
|
|
XM_011532800.1:c.3549_3570delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
XP_011531102.1:p.Thr1183=
|
|
XM_024452819.1:c.3939_3960delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
XP_024308587.1:p.Thr1313=
|
|
XM_024452820.1:c.3756_3777delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
XP_024308588.1:p.Thr1252=
|
|
XM_024452821.1:c.3642_3663delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
XP_024308589.1:p.Thr1214=
|
|
XM_024452822.1:c.3033_3054delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
XP_024308590.1:p.Thr1011=
|
|
NM_000179.3:c.3846_3867delinsTATTACGTTCCTCTATAAATTC
(MSH6)
MANE Select
|
NP_000170.1:p.Thr1282=
|
|
NM_001281492.2:c.3456_3477delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
NP_001268421.1:p.Thr1152=
|
|
NM_001281493.2:c.2940_2961delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
NP_001268422.1:p.Thr980=
|
|
NM_001281494.2:c.2940_2961delinsTATTACGTTCCTCTATAAATTC
(MSH6)
|
NP_001268423.1:p.Thr980=
|
|