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MANE Select
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ENSP00000359878.5:p.Met274=
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ENSP00000359878.4:p.Met274=
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ENSP00000442324.1:p.Met238=
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NM_000016.5:c.821T=
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NP_000007.1:p.Met274=
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NM_001127328.2:c.833T=
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NP_001120800.1:p.Met278=
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NM_001286042.1:c.713T=
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NP_001272971.1:p.Met238=
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NM_001286043.1:c.920T=
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NP_001272972.1:p.Met307=
|
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NM_001286044.1:c.254T=
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NP_001272973.1:p.Met85=
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NM_000016.6:c.821T=
MANE Select
|
NP_000007.1:p.Met274=
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NM_001127328.3:c.833T=
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NP_001120800.1:p.Met278=
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NM_001286042.2:c.713T=
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NP_001272971.1:p.Met238=
|
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NM_001286043.2:c.920T=
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NP_001272972.1:p.Met307=
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NM_001286044.2:c.254T=
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NP_001272973.1:p.Met85=
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