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ENST00000510025.7:c.1566T=
MANE Select
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NM_000414.3:c.1566T=
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NP_000405.1:p.Ser522=
|
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NM_001199291.2:c.1641T=
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NP_001186220.1:p.Ser547=
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NM_001199292.1:c.1512T=
|
NP_001186221.1:p.Ser504=
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NM_001292027.1:c.1494T=
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NP_001278956.1:p.Ser498=
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NM_001292028.1:c.1146T=
|
NP_001278957.1:p.Ser382=
|
|
NM_000414.4:c.1566T=
MANE Select
|
NP_000405.1:p.Ser522=
|
|
NM_001199291.3:c.1641T=
|
NP_001186220.1:p.Ser547=
|
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|
NP_001186221.1:p.Ser504=
|
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|
NP_001278956.1:p.Ser498=
|
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NM_001292028.2:c.1146T=
|
NP_001278957.1:p.Ser382=
|
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NM_001374497.1:c.1557T=
|
NP_001361426.1:p.Ser519=
|
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NM_001374498.1:c.1494T=
|
NP_001361427.1:p.Ser498=
|
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NM_001374499.1:c.1239T=
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NP_001361428.1:p.Ser413=
|
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NM_001374500.1:c.1125T=
|
NP_001361429.1:p.Ser375=
|
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NM_001374501.1:c.1155T=
|
NP_001361430.1:p.Ser385=
|
|
NM_001374502.1:c.1155T=
|
NP_001361431.1:p.Ser385=
|
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NM_001374503.1:c.1155T=
|
NP_001361432.1:p.Ser385=
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NR_164653.1:n.1663T=
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NR_164654.1:n.1931T=
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