ENST00000296684.10:c.33G>A
MANE Select
|
ENSP00000296684.5:p.Arg11=
|
|
ENST00000296684.9:c.33G>A
|
ENSP00000296684.5:p.Arg11=
|
|
ENST00000502423.5:c.33G>A
|
ENSP00000422177.1:p.Arg11=
|
|
ENST00000506765.1:c.21G>A
|
ENSP00000424570.1:p.Arg7=
|
|
ENST00000506974.5:c.33G>A
|
ENSP00000425967.1:p.Arg11=
|
|
ENST00000507026.5:c.33G>A
|
ENSP00000424993.1:p.Arg11=
|
|
NM_002495.2:c.33G>A
|
NP_002486.1:p.Arg11=
|
|
XM_005248525.3:c.33G>A
|
XP_005248582.1:p.Arg11=
|
|
XM_011543414.1:c.33G>A
|
XP_011541716.1:p.Arg11=
|
|
NM_001318051.1:c.33G>A
|
NP_001304980.1:p.Arg11=
|
|
NM_002495.3:c.33G>A
|
NP_002486.1:p.Arg11=
|
|
NR_134473.1:n.63G>A
|
|
|
NR_134474.1:n.63G>A
|
|
|
NR_134475.1:n.63G>A
|
|
|
XM_017009491.1:c.33G>A
|
XP_016864980.1:p.Arg11=
|
|
NM_002495.4:c.33G>A
MANE Select
|
NP_002486.1:p.Arg11=
|
|
NM_001318051.2:c.33G>A
|
NP_001304980.1:p.Arg11=
|
|
NR_134473.2:n.57G>A
|
|
|
NR_134474.2:n.57G>A
|
|
|
NR_134475.2:n.57G>A
|
|
|