ENST00000394867.9:n.1772G=
|
|
|
ENST00000688002.1:n.3484G=
|
|
|
ENST00000688751.1:n.469G=
|
|
|
ENST00000689792.1:n.1237G=
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|
|
ENST00000262948.10:c.*130G=
MANE Select
|
ENSP00000262948.4:n.*130G=
|
|
ENST00000262948.9:c.*130G=
|
ENSP00000262948.3:n.*130G=
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|
ENST00000394867.8:c.*130G=
|
ENSP00000378336.1:n.*130G=
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|
ENST00000597263.5:n.518G=
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|
|
ENST00000600584.5:n.2782G=
|
|
|
ENST00000601786.5:n.1634G=
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|
|
NM_030662.3:c.*130G= , LRG_750t1:c.*130G=
|
NP_109587.1:n.*130G=
|
|
XM_006722799.2:c.*130G=
|
XP_006722862.1:n.*130G=
|
|
XM_011528133.1:c.*130G=
|
XP_011526435.1:n.*130G=
|
|
NM_030662.4:c.*130G=
MANE Select
|
NP_109587.1:n.*130G=
|
|