ENST00000394867.9:n.1779G=
|
|
|
ENST00000688002.1:n.3491G=
|
|
|
ENST00000688751.1:n.476G=
|
|
|
ENST00000689792.1:n.1244G=
|
|
|
ENST00000262948.10:c.*137G=
MANE Select
|
ENSP00000262948.4:n.*137G=
|
|
ENST00000262948.9:c.*137G=
|
ENSP00000262948.3:n.*137G=
|
|
ENST00000394867.8:c.*137G=
|
ENSP00000378336.1:n.*137G=
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|
ENST00000597263.5:n.525G=
|
|
|
ENST00000600584.5:n.2789G=
|
|
|
ENST00000601786.5:n.1641G=
|
|
|
NM_030662.3:c.*137G= , LRG_750t1:c.*137G=
|
NP_109587.1:n.*137G=
|
|
XM_006722799.2:c.*137G=
|
XP_006722862.1:n.*137G=
|
|
XM_011528133.1:c.*137G=
|
XP_011526435.1:n.*137G=
|
|
NM_030662.4:c.*137G=
MANE Select
|
NP_109587.1:n.*137G=
|
|