ENST00000360215.3:c.414C>G
MANE Select
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ENSP00000353346.1:p.Ala138=
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|
ENST00000496656.2:n.193C>G
|
|
|
ENST00000651132.1:c.414C>G
|
ENSP00000498322.1:p.Ala138=
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|
ENST00000651676.1:c.414C>G
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ENSP00000498699.1:p.Ala138=
|
|
ENST00000651994.1:c.*70-4890C>G
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ENSP00000498310.1:n.*70-4890C>G
|
|
ENST00000652718.1:c.246C>G
|
ENSP00000498866.1:p.Ala82=
|
|
ENST00000360215.2:c.414C>G
|
ENSP00000353346.1:p.Ala138=
|
|
ENST00000496656.1:n.193C>G
|
|
|
NM_182548.3:c.414C>G
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NP_872354.1:p.Ala138=
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XM_011514403.1:c.414C>G
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XP_011512705.1:p.Ala138=
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|
NM_182548.4:c.414C>G
MANE Select
|
NP_872354.1:p.Ala138=
|
|