ENST00000394867.9:n.1583T>C
|
|
|
ENST00000688002.1:n.3295T>C
|
|
|
ENST00000688751.1:n.280T>C
|
|
|
ENST00000689792.1:n.1048T>C
|
|
|
ENST00000262948.10:c.1144T>C
MANE Select
|
ENSP00000262948.4:p.Trp382Arg
|
|
ENST00000262948.9:c.1144T>C
|
ENSP00000262948.3:p.Trp382Arg
|
|
ENST00000394867.8:c.853T>C
|
ENSP00000378336.1:p.Trp285Arg
|
|
ENST00000597263.5:n.329T>C
|
|
|
ENST00000599021.1:c.254T>C
|
|
|
ENST00000600584.5:n.2593T>C
|
|
|
ENST00000601786.5:n.1445T>C
|
|
|
NM_030662.3:c.1144T>C , LRG_750t1:c.1144T>C
|
NP_109587.1:p.Trp382Arg
|
|
XM_006722799.2:c.865T>C
|
XP_006722862.1:p.Trp289Arg
|
|
XM_011528133.1:c.574T>C
|
XP_011526435.1:p.Trp192Arg
|
|
NM_030662.4:c.1144T>C
MANE Select
|
NP_109587.1:p.Trp382Arg
|
|