ENST00000680821.2:c.3882G>T
MANE Select
|
ENSP00000504874.1:p.Gln1294His
|
|
ENST00000262765.10:c.3384G>T
|
ENSP00000262765.5:p.Gln1128His
|
|
ENST00000636395.1:c.3882G>T
|
ENSP00000490761.1:p.Gln1294His
|
|
ENST00000680821.1:c.3882G>T
|
ENSP00000504874.1:p.Gln1294His
|
|
ENST00000262765.9:c.3384G>T
|
ENSP00000262765.5:p.Gln1128His
|
|
ENST00000447564.2:c.408G>T
|
ENSP00000394461.2:p.Gln136His
|
|
ENST00000524722.1:c.*148G>T
|
ENSP00000432679.1:n.*148G>T
|
|
NM_032134.2:c.3384G>T
|
NP_115510.1:p.Gln1128His
|
|
NR_130649.1:n.655G>T
|
|
|
XM_005257728.2:c.3882G>T
|
XP_005257785.1:p.Gln1294His
|
|
XM_006722136.2:c.144G>T
|
XP_006722199.1:p.Gln48His
|
|
XM_011525344.1:c.3162G>T
|
XP_011523646.1:p.Gln1054His
|
|
XM_005257728.4:c.3882G>T
|
XP_005257785.1:p.Gln1294His
|
|
XM_006722136.3:c.144G>T
|
XP_006722199.1:p.Gln48His
|
|
XM_011525344.2:c.3162G>T
|
XP_011523646.1:p.Gln1054His
|
|
XM_017025206.2:c.3882G>T
|
XP_016880695.1:p.Gln1294His
|
|
XM_017025207.2:c.3822G>T
|
XP_016880696.1:p.Gln1274His
|
|
XM_017025208.1:c.-85G>T
|
XP_016880697.1:n.-85G>T
|
|
NM_001388453.1:c.3882G>T
MANE Select
|
NP_001375382.1:p.Gln1294His
|
|
NM_032134.3:c.3882G>T
|
NP_115510.2:p.Gln1294His
|
|
NR_130649.2:n.1251G>T
|
|
|