|
ENST00000394867.9:n.1660G=
|
|
|
|
ENST00000688002.1:n.3372G=
|
|
|
|
ENST00000688751.1:n.357G=
|
|
|
|
ENST00000689792.1:n.1125G=
|
|
|
|
ENST00000262948.10:c.*18G=
MANE Select
|
ENSP00000262948.4:n.*18G=
|
|
|
ENST00000262948.9:c.*18G=
|
ENSP00000262948.3:n.*18G=
|
|
|
ENST00000394867.8:c.*18G=
|
ENSP00000378336.1:n.*18G=
|
|
|
ENST00000597263.5:n.406G=
|
|
|
|
ENST00000600584.5:n.2670G=
|
|
|
|
ENST00000601786.5:n.1522G=
|
|
|
|
NM_030662.3:c.*18G= , LRG_750t1:c.*18G=
|
NP_109587.1:n.*18G=
|
|
|
XM_006722799.2:c.*18G=
|
XP_006722862.1:n.*18G=
|
|
|
XM_011528133.1:c.*18G=
|
XP_011526435.1:n.*18G=
|
|
|
NM_030662.4:c.*18G=
MANE Select
|
NP_109587.1:n.*18G=
|
|
