ENST00000394867.9:n.1721G=
|
|
|
ENST00000688002.1:n.3433G=
|
|
|
ENST00000688751.1:n.418G=
|
|
|
ENST00000689792.1:n.1186G=
|
|
|
ENST00000262948.10:c.*79G=
MANE Select
|
ENSP00000262948.4:n.*79G=
|
|
ENST00000262948.9:c.*79G=
|
ENSP00000262948.3:n.*79G=
|
|
ENST00000394867.8:c.*79G=
|
ENSP00000378336.1:n.*79G=
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|
ENST00000597263.5:n.467G=
|
|
|
ENST00000600584.5:n.2731G=
|
|
|
ENST00000601786.5:n.1583G=
|
|
|
NM_030662.3:c.*79G= , LRG_750t1:c.*79G=
|
NP_109587.1:n.*79G=
|
|
XM_006722799.2:c.*79G=
|
XP_006722862.1:n.*79G=
|
|
XM_011528133.1:c.*79G=
|
XP_011526435.1:n.*79G=
|
|
NM_030662.4:c.*79G=
MANE Select
|
NP_109587.1:n.*79G=
|
|