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ENST00000691629.1:n.1563C=
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ENST00000338154.11:c.2199C=
MANE Select
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ENSP00000338868.6:p.Ser733=
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ENST00000322659.12:c.2148C=
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ENSP00000319473.8:p.Ser716=
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ENST00000615775.4:c.626C=
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NM_001184896.1:c.2307C=
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NP_001171825.1:p.Ser769=
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NM_001184897.1:c.1896C=
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NM_001184898.1:c.2148C=
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NP_001171827.1:p.Ser716=
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NM_015107.2:c.2199C=
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NP_055922.1:p.Ser733=
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XM_005261996.1:c.2307C=
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XP_005262053.1:p.Ser769=
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XP_005262056.1:p.Ser733=
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XM_005262000.1:c.2004C=
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XM_006724585.1:c.2307C=
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XP_006724648.1:p.Ser769=
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XM_011530778.1:c.2307C=
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XP_011529080.1:p.Ser769=
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NM_001184898.2:c.2148C=
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NP_001171827.1:p.Ser716=
|
|
NM_015107.3:c.2199C=
MANE Select
|
NP_055922.1:p.Ser733=
|
|
NM_001184897.2:c.1896C=
|
NP_001171826.1:p.Ser632=
|
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