ENST00000394867.9:n.1702G=
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|
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ENST00000688002.1:n.3414G=
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ENST00000688751.1:n.399G=
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|
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ENST00000689792.1:n.1167G=
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|
|
ENST00000262948.10:c.*60G=
MANE Select
|
ENSP00000262948.4:n.*60G=
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ENST00000262948.9:c.*60G=
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ENSP00000262948.3:n.*60G=
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ENST00000394867.8:c.*60G=
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ENSP00000378336.1:n.*60G=
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ENST00000597263.5:n.448G=
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|
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ENST00000600584.5:n.2712G=
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|
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ENST00000601786.5:n.1564G=
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|
|
NM_030662.3:c.*60G= , LRG_750t1:c.*60G=
|
NP_109587.1:n.*60G=
|
|
XM_006722799.2:c.*60G=
|
XP_006722862.1:n.*60G=
|
|
XM_011528133.1:c.*60G=
|
XP_011526435.1:n.*60G=
|
|
NM_030662.4:c.*60G=
MANE Select
|
NP_109587.1:n.*60G=
|
|