ENST00000269260.7:c.852G>T
MANE Select
|
ENSP00000269260.2:p.Glu284Asp
|
|
ENST00000269260.6:c.852G>T
|
ENSP00000269260.2:p.Glu284Asp
|
|
ENST00000346341.6:c.807G>T
|
ENSP00000341895.2:p.Glu269Asp
|
|
ENST00000381488.10:c.807G>T
|
ENSP00000370898.6:p.Glu269Asp
|
|
ENST00000412477.7:c.915G>T
|
ENSP00000403701.3:p.Glu305Asp
|
|
ENST00000571206.1:c.276G>T
|
ENSP00000460607.1:p.Glu92Asp
|
|
ENST00000571428.5:c.276G>T
|
ENSP00000465877.1:p.Glu92Asp
|
|
ENST00000572457.5:c.276G>T
|
ENSP00000465296.1:p.Glu92Asp
|
|
ENST00000574502.5:c.*330G>T
|
ENSP00000458371.1:n.*330G>T
|
|
ENST00000574954.5:c.276G>T
|
ENSP00000466344.1:p.Glu92Asp
|
|
ENST00000575877.5:c.786+66G>T
|
ENSP00000466857.1:n.786+66G>T
|
|
ENST00000576235.1:c.734G>T
|
ENSP00000460879.1:n.734G>T
|
|
NM_001257328.1:c.915G>T
|
NP_001244257.1:p.Glu305Asp
|
|
NM_001257329.1:c.786+66G>T
|
NP_001244258.1:n.786+66G>T
|
|
NM_001257330.1:c.852G>T
|
NP_001244259.1:p.Glu284Asp
|
|
NM_001257331.1:c.807G>T
|
NP_001244260.1:p.Glu269Asp
|
|
NM_004313.3:c.852G>T
|
NP_004304.1:p.Glu284Asp
|
|
NM_199004.1:c.807G>T
|
NP_945355.1:p.Glu269Asp
|
|
NR_047516.1:n.1049G>T
|
|
|
XM_006721520.1:c.276G>T
|
XP_006721583.1:p.Glu92Asp
|
|
XM_006721521.1:c.276G>T
|
XP_006721584.1:p.Glu92Asp
|
|
XM_011523858.1:c.945G>T
|
XP_011522160.1:p.Glu315Asp
|
|
XM_011523859.1:c.900G>T
|
XP_011522161.1:p.Glu300Asp
|
|
NM_001330064.1:c.276G>T
|
NP_001316993.1:p.Glu92Asp
|
|
XM_011523858.2:c.945G>T
|
XP_011522160.1:p.Glu315Asp
|
|
XM_017024645.1:c.276G>T
|
XP_016880134.1:p.Glu92Asp
|
|
XM_024450751.1:c.852G>T
|
XP_024306519.1:p.Glu284Asp
|
|
XM_024450752.1:c.276G>T
|
XP_024306520.1:p.Glu92Asp
|
|
XM_024450753.1:c.276G>T
|
XP_024306521.1:p.Glu92Asp
|
|
XR_002958006.1:n.859G>T
|
|
|
XR_002958007.1:n.859G>T
|
|
|
NM_004313.4:c.852G>T
MANE Select
|
NP_004304.1:p.Glu284Asp
|
|
NM_001257328.2:c.915G>T
|
NP_001244257.1:p.Glu305Asp
|
|
NM_001257329.2:c.786+66G>T
|
NP_001244258.1:n.786+66G>T
|
|
NM_001257330.2:c.852G>T
|
NP_001244259.1:p.Glu284Asp
|
|
NM_001257331.2:c.807G>T
|
NP_001244260.1:p.Glu269Asp
|
|
NM_001330064.2:c.276G>T
|
NP_001316993.1:p.Glu92Asp
|
|
NM_199004.2:c.807G>T
|
NP_945355.1:p.Glu269Asp
|
|
NR_047516.2:n.911G>T
|
|
|