ENST00000371757.7:c.1650G>T
MANE Select
|
ENSP00000360822.2:p.Gln550His
|
|
ENST00000674572.1:c.1491G>T
|
ENSP00000501742.1:p.Gln497His
|
|
ENST00000675090.1:c.1398G>T
|
ENSP00000501833.1:p.Gln466His
|
|
ENST00000675399.1:c.1398G>T
|
ENSP00000501932.1:p.Gln466His
|
|
ENST00000676421.1:c.1407G>T
|
ENSP00000502322.1:p.Gln469His
|
|
ENST00000263604.5:c.1551G>T
|
ENSP00000263604.4:p.Gln517His
|
|
ENST00000371757.6:c.1650G>T
|
ENSP00000360822.2:p.Gln550His
|
|
ENST00000460750.5:c.*1260G>T
|
ENSP00000418777.1:n.*1260G>T
|
|
ENST00000486577.6:c.1533G>T
|
ENSP00000417578.3:p.Gln511His
|
|
ENST00000487664.5:c.1650G>T
|
ENSP00000417851.2:p.Gln550His
|
|
ENST00000488444.6:c.1593G>T
|
ENSP00000419007.3:p.Gln531His
|
|
ENST00000490355.6:c.1593G>T
|
ENSP00000418003.3:p.Gln531His
|
|
ENST00000490363.3:n.1469G>T
|
|
|
ENST00000491806.6:c.1593G>T
|
ENSP00000419086.3:p.Gln531His
|
|
ENST00000628528.2:c.1515G>T
|
ENSP00000486374.1:p.Gln505His
|
|
ENST00000630792.2:c.1491G>T
|
ENSP00000486486.1:p.Gln497His
|
|
ENST00000631073.2:c.1593G>T
|
ENSP00000486130.1:p.Gln531His
|
|
NM_001272003.1:c.1515G>T
|
NP_001258932.1:p.Gln505His
|
|
NM_020822.2:c.1650G>T
|
NP_065873.2:p.Gln550His
|
|
XM_011518877.1:c.1785G>T
|
XP_011517179.1:p.Gln595His
|
|
XM_011518878.1:c.1794G>T
|
XP_011517180.1:p.Gln598His
|
|
XM_011518879.1:c.1785G>T
|
XP_011517181.1:p.Gln595His
|
|
XM_011518880.1:c.1551G>T
|
XP_011517182.1:p.Gln517His
|
|
XM_011518881.1:c.1140G>T
|
XP_011517183.1:p.Gln380His
|
|
XM_011518877.3:c.1785G>T
|
XP_011517179.1:p.Gln595His
|
|
XM_011518878.3:c.1794G>T
|
XP_011517180.1:p.Gln598His
|
|
XM_011518879.3:c.1785G>T
|
XP_011517181.1:p.Gln595His
|
|
XM_011518881.3:c.1140G>T
|
XP_011517183.1:p.Gln380His
|
|
XM_017014931.1:c.1584G>T
|
XP_016870420.1:p.Gln528His
|
|
XM_017014932.1:c.1407G>T
|
XP_016870421.1:p.Gln469His
|
|
XM_017014933.1:c.1140G>T
|
XP_016870422.1:p.Gln380His
|
|
XM_024447617.1:c.1140G>T
|
XP_024303385.1:p.Gln380His
|
|
XM_024447618.1:c.1140G>T
|
XP_024303386.1:p.Gln380His
|
|
NM_020822.3:c.1650G>T
MANE Select
|
NP_065873.2:p.Gln550His
|
|
NM_001272003.2:c.1515G>T
|
NP_001258932.1:p.Gln505His
|
|