ENST00000276079.13:c.1302C>T
MANE Select
|
ENSP00000276079.8:p.Arg434=
|
|
ENST00000373856.8:c.1400C>T
|
ENSP00000362963.4:p.Ala467Val
|
|
ENST00000420903.6:c.1302C>T
|
ENSP00000410299.2:p.Arg434=
|
|
ENST00000450092.6:c.1302C>T
|
ENSP00000415777.2:p.Arg434=
|
|
ENST00000454976.2:c.1302C>T
|
ENSP00000406673.2:p.Arg434=
|
|
ENST00000473525.2:n.2010C>T
|
|
|
ENST00000676495.1:n.2713C>T
|
|
|
ENST00000676499.1:n.2258C>T
|
|
|
ENST00000676797.1:c.1035C>T
|
ENSP00000503920.1:p.Arg345=
|
|
ENST00000677014.1:c.*1129C>T
|
ENSP00000503813.1:n.*1129C>T
|
|
ENST00000677218.1:n.2473C>T
|
|
|
ENST00000677245.1:c.*1511C>T
|
ENSP00000503929.1:n.*1511C>T
|
|
ENST00000677274.1:c.1302C>T
|
ENSP00000504314.1:p.Arg434=
|
|
ENST00000677446.1:c.1302C>T
|
ENSP00000503031.1:p.Arg434=
|
|
ENST00000677612.1:c.1302C>T
|
ENSP00000504351.1:p.Arg434=
|
|
ENST00000677766.1:n.3707C>T
|
|
|
ENST00000677826.1:n.2044C>T
|
|
|
ENST00000677879.1:c.1122C>T
|
ENSP00000504090.1:p.Arg374=
|
|
ENST00000677977.1:n.3134C>T
|
|
|
ENST00000678231.1:c.1302C>T
|
ENSP00000503233.1:p.Arg434=
|
|
ENST00000678323.1:n.2400C>T
|
|
|
ENST00000678335.1:c.*215C>T
|
ENSP00000503769.1:n.*215C>T
|
|
ENST00000678437.1:c.1293C>T
|
ENSP00000504007.1:p.Arg431=
|
|
ENST00000678660.1:c.1317C>T
|
ENSP00000504665.1:p.Arg439=
|
|
ENST00000678830.1:c.1392C>T
|
ENSP00000504263.1:p.Arg464=
|
|
ENST00000679029.1:c.*116C>T
|
ENSP00000504193.1:n.*116C>T
|
|
ENST00000679267.1:n.3509C>T
|
|
|
ENST00000276079.12:c.1302C>T
|
ENSP00000276079.8:p.Arg434=
|
|
ENST00000373841.5:c.1302C>T
|
ENSP00000362947.1:p.Arg434=
|
|
ENST00000373856.7:c.1302C>T
|
ENSP00000362963.3:p.Arg434=
|
|
ENST00000472185.1:n.61-557C>T
|
|
|
ENST00000473525.1:n.1076C>T
|
|
|
ENST00000474431.5:n.337C>T
|
|
|
ENST00000490044.5:n.2009C>T
|
|
|
ENST00000535149.5:c.1035C>T
|
ENSP00000441364.1:p.Arg345=
|
|
NM_001145408.1:c.1302C>T
|
NP_001138880.1:p.Arg434=
|
|
NM_001145409.1:c.1302C>T
|
NP_001138881.1:p.Arg434=
|
|
NM_001145410.1:c.1035C>T
|
NP_001138882.1:p.Arg345=
|
|
NM_007363.4:c.1302C>T
|
NP_031389.3:p.Arg434=
|
|
NM_007363.5:c.1302C>T
MANE Select
|
NP_031389.3:p.Arg434=
|
|
NM_001145408.2:c.1302C>T
|
NP_001138880.1:p.Arg434=
|
|
NM_001145409.2:c.1302C>T
|
NP_001138881.1:p.Arg434=
|
|
NM_001145410.2:c.1035C>T
|
NP_001138882.1:p.Arg345=
|
|