ENST00000394867.9:n.1491T=
|
|
|
ENST00000688002.1:n.3203T=
|
|
|
ENST00000688751.1:n.188T=
|
|
|
ENST00000689792.1:n.956T=
|
|
|
ENST00000262948.10:c.1052T=
MANE Select
|
ENSP00000262948.4:p.Ile351=
|
|
ENST00000262948.9:c.1052T=
|
ENSP00000262948.3:p.Ile351=
|
|
ENST00000394867.8:c.761T=
|
ENSP00000378336.1:p.Ile254=
|
|
ENST00000597263.5:n.237T=
|
|
|
ENST00000599021.1:c.162T=
|
|
|
ENST00000600584.5:n.2501T=
|
|
|
ENST00000601786.5:n.1353T=
|
|
|
NM_030662.3:c.1052T= , LRG_750t1:c.1052T=
|
NP_109587.1:p.Ile351=
|
|
XM_006722799.2:c.773T=
|
XP_006722862.1:p.Ile258=
|
|
XM_011528133.1:c.482T=
|
XP_011526435.1:p.Ile161=
|
|
NM_030662.4:c.1052T=
MANE Select
|
NP_109587.1:p.Ile351=
|
|