ENST00000305544.9:c.2661C=
MANE Select
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ENSP00000307156.4:p.Asn887=
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ENST00000305544.8:c.2661C=
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ENSP00000307156.4:p.Asn887=
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|
ENST00000418109.5:c.2661C=
|
ENSP00000388325.1:p.Asn887=
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ENST00000462930.5:n.68C=
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ENST00000464891.5:n.410C=
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ENST00000477701.1:n.534C=
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ENST00000483057.1:n.261C=
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|
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ENST00000486298.5:n.426-143C=
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|
|
NM_002292.3:c.2661C=
|
NP_002283.3:p.Asn887=
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XM_005265127.3:c.2661C=
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XP_005265184.1:p.Asn887=
|
|
XM_005265127.4:c.2661C=
|
XP_005265184.1:p.Asn887=
|
|
NM_002292.4:c.2661C=
MANE Select
|
NP_002283.3:p.Asn887=
|
|