ENST00000563588.6:c.508T=
MANE Select
|
ENSP00000455607.1:p.Ser170=
|
|
ENST00000328273.11:c.508T=
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ENSP00000329968.7:p.Ser170=
|
|
ENST00000424889.7:c.508T=
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ENSP00000388571.3:p.Ser170=
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|
ENST00000561712.1:c.182T=
|
|
|
ENST00000563588.5:c.508T=
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ENSP00000455607.1:p.Ser170=
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|
ENST00000563607.1:c.*180T=
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ENSP00000454641.1:n.*180T=
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ENST00000563913.5:n.841T=
|
|
|
ENST00000564838.5:n.882T=
|
|
|
ENST00000565897.5:c.508T=
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ENSP00000457359.1:p.Ser170=
|
|
ENST00000565924.5:c.508T=
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ENSP00000455091.1:p.Ser170=
|
|
ENST00000569684.1:n.920T=
|
|
|
NM_000294.2:c.508T=
|
NP_000285.1:p.Ser170=
|
|
NM_001172432.1:c.508T=
|
NP_001165903.1:p.Ser170=
|
|
NM_000294.3:c.508T=
MANE Select
|
NP_000285.1:p.Ser170=
|
|
NM_001172432.2:c.508T=
|
NP_001165903.1:p.Ser170=
|
|