ENST00000261208.8:c.1305G>A
MANE Select
|
ENSP00000261208.3:p.Arg435=
|
|
ENST00000261208.7:c.1305G>A
|
ENSP00000261208.3:p.Arg435=
|
|
ENST00000538703.5:c.1305G>A
|
ENSP00000440861.1:p.Arg435=
|
|
ENST00000541929.5:c.681G>A
|
ENSP00000446364.1:p.Arg227=
|
|
ENST00000544080.6:c.*734G>A
|
ENSP00000439385.2:n.*734G>A
|
|
ENST00000546999.5:c.*734G>A
|
ENSP00000447675.1:n.*734G>A
|
|
NM_001258333.1:c.681G>A
|
NP_001245262.1:p.Arg227=
|
|
NM_001258334.1:c.1305G>A
|
NP_001245263.1:p.Arg435=
|
|
NM_002108.3:c.1305G>A
|
NP_002099.1:p.Arg435=
|
|
XM_011538249.1:c.453G>A
|
XP_011536551.1:p.Arg151=
|
|
XM_011538249.2:c.453G>A
|
XP_011536551.1:p.Arg151=
|
|
XM_017019246.1:c.375G>A
|
XP_016874735.1:p.Arg125=
|
|
NM_002108.4:c.1305G>A
MANE Select
|
NP_002099.1:p.Arg435=
|
|
NM_001258334.2:c.1305G>A
|
NP_001245263.1:p.Arg435=
|
|
NM_001258333.2:c.681G>A
|
NP_001245262.1:p.Arg227=
|
|