ENST00000650516.2:c.893C=
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ENSP00000498052.2:p.Ala298=
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ENST00000343257.7:c.893C=
MANE Select
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ENSP00000339867.2:p.Ala298=
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ENST00000432192.6:c.717C=
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ENST00000455478.6:c.481C=
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ENSP00000400027.2:n.481C=
|
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ENST00000650516.1:c.893C=
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ENSP00000498052.1:p.Ala298=
|
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ENST00000343257.6:c.893C=
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ENSP00000339867.2:p.Ala298=
|
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ENST00000432192.5:c.407C=
|
|
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ENST00000455478.5:c.485C=
|
|
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ENST00000495612.1:n.194C=
|
|
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NM_000083.2:c.893C=
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NP_000074.2:p.Ala298=
|
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NR_046453.1:n.983C=
|
|
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XM_011515781.1:c.893C=
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XP_011514083.1:p.Ala298=
|
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XM_017011739.1:c.443C=
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XP_016867228.1:p.Ala148=
|
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XM_017011740.1:c.443C=
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XP_016867229.1:p.Ala148=
|
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NM_000083.3:c.893C=
MANE Select
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NP_000074.3:p.Ala298=
|
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NR_046453.2:n.998C=
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