ENST00000394867.9:n.1613C=
|
|
|
ENST00000688002.1:n.3325C=
|
|
|
ENST00000688751.1:n.310C=
|
|
|
ENST00000689792.1:n.1078C=
|
|
|
ENST00000262948.10:c.1174C=
MANE Select
|
ENSP00000262948.4:p.Pro392=
|
|
ENST00000262948.9:c.1174C=
|
ENSP00000262948.3:p.Pro392=
|
|
ENST00000394867.8:c.883C=
|
ENSP00000378336.1:p.Pro295=
|
|
ENST00000597263.5:n.359C=
|
|
|
ENST00000599021.1:c.284C=
|
|
|
ENST00000600584.5:n.2623C=
|
|
|
ENST00000601786.5:n.1475C=
|
|
|
NM_030662.3:c.1174C= , LRG_750t1:c.1174C=
|
NP_109587.1:p.Pro392=
|
|
XM_006722799.2:c.895C=
|
XP_006722862.1:p.Pro299=
|
|
XM_011528133.1:c.604C=
|
XP_011526435.1:p.Pro202=
|
|
NM_030662.4:c.1174C=
MANE Select
|
NP_109587.1:p.Pro392=
|
|