|
ENST00000528025.6:c.1192C>T
|
ENSP00000437303.2:p.Gln398Ter
|
|
|
ENST00000685198.1:c.1111C>T
|
ENSP00000510528.1:p.Gln371Ter
|
|
|
ENST00000687971.1:c.778C>T
|
ENSP00000510788.1:p.Gln260Ter
|
|
|
ENST00000693060.1:c.991C>T
|
ENSP00000510329.1:p.Gln331Ter
|
|
|
ENST00000345136.8:c.1060C>T
MANE Select
|
ENSP00000344848.3:p.Gln354Ter
|
|
|
ENST00000527303.2:c.1141C>T
|
ENSP00000433982.2:p.Gln381Ter
|
|
|
ENST00000322810.8:c.1471C>T
|
ENSP00000323856.4:p.Gln491Ter
|
|
|
ENST00000345136.7:c.1060C>T
|
ENSP00000344848.3:p.Gln354Ter
|
|
|
ENST00000354589.7:c.1060C>T
|
ENSP00000346602.3:p.Gln354Ter
|
|
|
ENST00000354958.6:c.994C>T
|
ENSP00000347044.2:p.Gln332Ter
|
|
|
ENST00000356346.7:c.1018C>T
MANE Plus Clinical
|
ENSP00000348702.3:p.Gln340Ter
|
|
|
ENST00000357649.6:c.1072C>T
|
ENSP00000350277.2:p.Gln358Ter
|
|
|
ENST00000398774.6:c.964C>T
|
ENSP00000381756.2:p.Gln322Ter
|
|
|
ENST00000436759.6:c.1141C>T
|
ENSP00000388180.2:p.Gln381Ter
|
|
|
ENST00000527096.5:c.1129C>T
|
ENSP00000434583.1:p.Gln377Ter
|
|
|
ENST00000528025.5:c.1192C>T
|
ENSP00000437303.1:p.Gln398Ter
|
|
|
NM_000445.4:c.1141C>T
|
NP_000436.2:p.Gln381Ter
|
|
|
NM_201378.3:c.1018C>T
|
NP_958780.1:p.Gln340Ter
|
|
|
NM_201379.2:c.994C>T
|
NP_958781.1:p.Gln332Ter
|
|
|
NM_201380.3:c.1471C>T
|
NP_958782.1:p.Gln491Ter
|
|
|
NM_201381.2:c.964C>T
|
NP_958783.1:p.Gln322Ter
|
|
|
NM_201382.3:c.1060C>T
|
NP_958784.1:p.Gln354Ter
|
|
|
NM_201383.2:c.1072C>T
|
NP_958785.1:p.Gln358Ter
|
|
|
NM_201384.2:c.1060C>T
|
NP_958786.1:p.Gln354Ter
|
|
|
XM_005250976.2:c.1486C>T
|
XP_005251033.1:p.Gln496Ter
|
|
|
XM_005250978.2:c.1087C>T
|
XP_005251035.1:p.Gln363Ter
|
|
|
XM_005250979.3:c.1075C>T
|
XP_005251036.1:p.Gln359Ter
|
|
|
XM_005250980.3:c.1075C>T
|
XP_005251037.1:p.Gln359Ter
|
|
|
XM_005250981.2:c.1033C>T
|
XP_005251038.1:p.Gln345Ter
|
|
|
XM_005250982.2:c.1009C>T
|
XP_005251039.1:p.Gln337Ter
|
|
|
XM_005250983.2:c.991C>T
|
XP_005251040.1:p.Gln331Ter
|
|
|
XM_005250984.3:c.979C>T
|
XP_005251041.1:p.Gln327Ter
|
|
|
XM_006716588.2:c.1156C>T
|
XP_006716651.1:p.Gln386Ter
|
|
|
XM_006716589.2:c.1006C>T
|
XP_006716652.1:p.Gln336Ter
|
|
|
XM_006716590.2:c.1006C>T
|
XP_006716653.1:p.Gln336Ter
|
|
|
XM_011517130.1:c.1075C>T
|
XP_011515432.1:p.Gln359Ter
|
|
|
XM_011517131.1:c.991C>T
|
XP_011515433.1:p.Gln331Ter
|
|
|
XM_011517132.1:c.1087C>T
|
XP_011515434.1:p.Gln363Ter
|
|
|
XM_005250976.4:c.1486C>T
|
XP_005251033.1:p.Gln496Ter
|
|
|
XM_005250978.3:c.1087C>T
|
XP_005251035.1:p.Gln363Ter
|
|
|
XM_005250979.4:c.1075C>T
|
XP_005251036.1:p.Gln359Ter
|
|
|
XM_005250980.4:c.1075C>T
|
XP_005251037.1:p.Gln359Ter
|
|
|
XM_005250981.3:c.1033C>T
|
XP_005251038.1:p.Gln345Ter
|
|
|
XM_005250982.4:c.1009C>T
|
XP_005251039.1:p.Gln337Ter
|
|
|
XM_005250984.5:c.979C>T
|
XP_005251041.1:p.Gln327Ter
|
|
|
XM_006716588.3:c.1156C>T
|
XP_006716651.1:p.Gln386Ter
|
|
|
XM_006716590.3:c.1006C>T
|
XP_006716653.1:p.Gln336Ter
|
|
|
XM_011517130.2:c.1075C>T
|
XP_011515432.1:p.Gln359Ter
|
|
|
XM_011517131.2:c.991C>T
|
XP_011515433.1:p.Gln331Ter
|
|
|
XM_011517132.2:c.1087C>T
|
XP_011515434.1:p.Gln363Ter
|
|
|
NM_000445.5:c.1141C>T
|
NP_000436.2:p.Gln381Ter
|
|
|
NM_201378.4:c.1018C>T
MANE Plus Clinical
|
NP_958780.1:p.Gln340Ter
|
|
|
NM_201379.3:c.994C>T
|
NP_958781.1:p.Gln332Ter
|
|
|
NM_201380.4:c.1471C>T
|
NP_958782.1:p.Gln491Ter
|
|
|
NM_201381.3:c.964C>T
|
NP_958783.1:p.Gln322Ter
|
|
|
NM_201382.4:c.1060C>T
|
NP_958784.1:p.Gln354Ter
|
|
|
NM_201383.3:c.1072C>T
|
NP_958785.1:p.Gln358Ter
|
|
|
NM_201384.3:c.1060C>T
MANE Select
|
NP_958786.1:p.Gln354Ter
|
|
