ENST00000394867.9:n.1809T=
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ENST00000688751.1:n.506T=
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ENST00000689792.1:n.1274T=
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ENST00000262948.10:c.*167T=
MANE Select
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ENSP00000262948.4:n.*167T=
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ENST00000262948.9:c.*167T=
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ENSP00000262948.3:n.*167T=
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ENST00000394867.8:c.*167T=
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ENSP00000378336.1:n.*167T=
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ENST00000600584.5:n.2819T=
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ENST00000601786.5:n.1671T=
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NM_030662.3:c.*167T= , LRG_750t1:c.*167T=
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NP_109587.1:n.*167T=
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XM_006722799.2:c.*167T=
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XP_006722862.1:n.*167T=
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XM_011528133.1:c.*167T=
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XP_011526435.1:n.*167T=
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NM_030662.4:c.*167T=
MANE Select
|
NP_109587.1:n.*167T=
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