ENST00000320650.9:c.*328T=
MANE Select
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ENSP00000323505.4:n.*328T=
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ENST00000296545.11:c.*328T=
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ENSP00000296545.7:n.*328T=
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ENST00000320650.8:c.*328T=
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ENSP00000323505.4:n.*328T=
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ENST00000394159.2:c.736T=
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ENSP00000377714.1:n.736T=
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ENST00000477265.5:c.*328T=
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ENSP00000436914.1:n.*328T=
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ENST00000514653.5:c.*328T=
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ENSP00000422271.1:n.*328T=
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NM_000585.4:c.*328T=
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NP_000576.1:n.*328T=
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NM_172175.2:c.*328T=
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NP_751915.1:n.*328T=
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NR_037840.2:n.1667T=
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|
|
NM_000585.5:c.*328T=
MANE Select
|
NP_000576.1:n.*328T=
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|
NM_172175.3:c.*328T=
|
NP_751915.1:n.*328T=
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NR_037840.3:n.1680T=
|
|
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