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ENST00000684743.1:n.6708C=
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ENST00000260665.12:c.3963C=
MANE Select
|
ENSP00000260665.7:p.Tyr1321=
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ENST00000260665.11:c.3963C=
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ENSP00000260665.7:p.Tyr1321=
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NM_133259.3:c.3963C=
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XM_006711915.2:c.3885C=
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XP_006711978.1:p.Tyr1295=
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XM_011532473.1:c.3888C=
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XP_011530775.1:p.Tyr1296=
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XM_011532474.1:c.3963C=
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XP_011530776.1:p.Tyr1321=
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XP_016858606.1:p.Tyr1270=
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XR_002958896.1:n.4005C=
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NM_133259.4:c.3963C=
MANE Select
|
NP_573566.2:p.Tyr1321=
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