ENST00000542664.4:c.483C>A
MANE Select
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ENSP00000437737.1:p.Ala161=
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ENST00000543956.5:c.-7C>A
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ENSP00000441861.2:n.-7C>A
|
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ENST00000378688.8:c.483C>A
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ENSP00000367959.3:p.Ala161=
|
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ENST00000542664.3:c.483C>A
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ENSP00000437737.1:p.Ala161=
|
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ENST00000543956.4:c.231C>A
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ENSP00000441861.1:p.Ala77=
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NM_000621.4:c.483C>A
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NP_000612.1:p.Ala161=
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NM_001165947.2:c.231C>A
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NP_001159419.1:p.Ala77=
|
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NM_000621.5:c.483C>A
MANE Select
|
NP_000612.1:p.Ala161=
|
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NM_001165947.5:c.-7C>A
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NP_001159419.2:n.-7C>A
|
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NM_001378924.1:c.483C>A
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NP_001365853.1:p.Ala161=
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