|
ENST00000442597.6:c.497T>C
(NME6)
MANE Select
|
ENSP00000406642.1:p.Val166Ala
|
|
|
ENST00000451657.6:c.457T>C
(NME6)
|
ENSP00000407933.1:p.Cys153Arg
|
|
|
ENST00000642710.1:c.203T>C
(NME6)
|
ENSP00000494272.1:p.Val68Ala
|
|
|
ENST00000643011.1:c.281T>C
(NME6)
|
ENSP00000496560.1:p.Val94Ala
|
|
|
ENST00000643457.1:c.497T>C
(NME6)
|
ENSP00000495130.1:p.Val166Ala
|
|
|
ENST00000412564.5:c.224-4254A>G
(ZNF589)
|
ENSP00000404398.1:n.224-4254A>G
|
|
|
ENST00000415053.5:c.497T>C
(NME6)
|
ENSP00000399582.1:p.Val166Ala
|
|
|
ENST00000415644.5:c.296T>C
(NME6)
|
ENSP00000394232.1:p.Val99Ala
|
|
|
ENST00000418431.5:c.*326T>C
(NME6)
|
ENSP00000394128.1:n.*326T>C
|
|
|
ENST00000421967.5:c.521T>C
(NME6)
|
ENSP00000416658.1:p.Val174Ala
|
|
|
ENST00000425930.5:c.497T>C
(NME6)
|
ENSP00000411116.1:p.Val166Ala
|
|
|
ENST00000426689.6:c.497T>C
(NME6)
|
ENSP00000440286.1:p.Val166Ala
|
|
|
ENST00000435684.5:c.457T>C
(NME6)
|
ENSP00000393261.1:p.Cys153Arg
|
|
|
ENST00000442597.5:c.497T>C
(NME6)
|
ENSP00000406642.1:p.Val166Ala
|
|
|
ENST00000444069.5:n.324T>C
(NME6)
|
|
|
|
ENST00000447314.5:c.362T>C
(NME6)
|
ENSP00000414842.1:p.Val121Ala
|
|
|
ENST00000451657.5:c.457T>C
(NME6)
|
ENSP00000407933.1:p.Cys153Arg
|
|
|
ENST00000452211.5:c.497T>C
(NME6)
|
ENSP00000392352.1:p.Val166Ala
|
|
|
NM_001308426.1:c.497T>C
(NME6)
|
NP_001295355.1:p.Val166Ala
|
|
|
NM_001308427.1:c.497T>C
(NME6)
|
NP_001295356.1:p.Val166Ala
|
|
|
NM_001308428.1:c.497T>C
(NME6)
|
NP_001295357.1:p.Val166Ala
|
|
|
NM_001308430.1:c.481T>C
(NME6)
|
NP_001295359.1:p.Cys161Arg
|
|
|
NM_001308431.1:c.457T>C
(NME6)
|
NP_001295360.1:p.Cys153Arg
|
|
|
NM_001308433.1:c.457T>C
(NME6)
|
NP_001295362.1:p.Cys153Arg
|
|
|
NM_001308434.1:c.362T>C
(NME6)
|
NP_001295363.1:p.Val121Ala
|
|
|
NM_001308435.1:c.296T>C
(NME6)
|
NP_001295364.1:p.Val99Ala
|
|
|
NM_005793.3:c.521T>C
(NME6)
|
NP_005784.1:p.Val174Ala
|
|
|
NM_005793.4:c.521T>C
(NME6)
|
NP_005784.1:p.Val174Ala
|
|
|
XM_005264789.2:c.971T>C
(NME6)
|
XP_005264846.1:p.Val324Ala
|
|
|
XM_005264790.2:c.931T>C
(NME6)
|
XP_005264847.1:p.Cys311Arg
|
|
|
XR_245088.2:n.1476T>C
(NME6)
|
|
|
|
XM_017005511.2:c.354+374T>C
(NME6)
|
XP_016861000.1:n.354+374T>C
|
|
|
XM_017005512.2:c.731T>C
(NME6)
|
XP_016861001.1:p.Val244Ala
|
|
|
XM_017005513.2:c.509T>C
(NME6)
|
XP_016861002.1:p.Val170Ala
|
|
|
XM_017005514.2:c.497T>C
(NME6)
|
XP_016861003.1:p.Val166Ala
|
|
|
XM_017005515.1:c.457T>C
(NME6)
|
XP_016861004.1:p.Cys153Arg
|
|
|
XM_017005516.2:c.378+374T>C
(NME6)
|
XP_016861005.1:n.378+374T>C
|
|
|
XM_017005517.1:c.281T>C
(NME6)
|
XP_016861006.1:p.Val94Ala
|
|
|
XM_017005518.2:c.272T>C
(NME6)
|
XP_016861007.1:p.Val91Ala
|
|
|
XM_024453297.1:c.394+374T>C
(NME6)
|
XP_024309065.1:n.394+374T>C
|
|
|
XM_024453298.1:c.628+374T>C
(NME6)
|
XP_024309066.1:n.628+374T>C
|
|
|
XM_024453299.1:c.526+374T>C
(NME6)
|
XP_024309067.1:n.526+374T>C
|
|
|
XM_024453300.1:c.418+374T>C
(NME6)
|
XP_024309068.1:n.418+374T>C
|
|
|
XM_024453301.1:c.406+374T>C
(NME6)
|
XP_024309069.1:n.406+374T>C
|
|
|
XM_024453302.1:c.394+374T>C
(NME6)
|
XP_024309070.1:n.394+374T>C
|
|
|
XM_024453303.1:c.394+374T>C
(NME6)
|
XP_024309071.1:n.394+374T>C
|
|
|
XM_024453304.1:c.394+374T>C
(NME6)
|
XP_024309072.1:n.394+374T>C
|
|
|
XM_024453305.1:c.394+374T>C
(NME6)
|
XP_024309073.1:n.394+374T>C
|
|
|
XM_024453306.1:c.394+374T>C
(NME6)
|
XP_024309074.1:n.394+374T>C
|
|
|
NM_001308426.2:c.497T>C
(NME6)
MANE Select
|
NP_001295355.1:p.Val166Ala
|
|
|
NM_001308427.2:c.497T>C
(NME6)
|
NP_001295356.1:p.Val166Ala
|
|
|
NM_001308428.2:c.497T>C
(NME6)
|
NP_001295357.1:p.Val166Ala
|
|
|
NM_001308430.2:c.481T>C
(NME6)
|
NP_001295359.1:p.Cys161Arg
|
|
|
NM_001308431.2:c.457T>C
(NME6)
|
NP_001295360.1:p.Cys153Arg
|
|
|
NM_001308433.2:c.457T>C
(NME6)
|
NP_001295362.1:p.Cys153Arg
|
|
|
NM_001308434.2:c.362T>C
(NME6)
|
NP_001295363.1:p.Val121Ala
|
|
|
NM_001308435.2:c.296T>C
(NME6)
|
NP_001295364.1:p.Val99Ala
|
|
|
NM_005793.5:c.521T>C
(NME6)
|
NP_005784.1:p.Val174Ala
|
|
