ENST00000360215.3:c.533C>T
MANE Select
|
ENSP00000353346.1:p.Ala178Val
|
|
ENST00000496656.2:n.312C>T
|
|
|
ENST00000651132.1:c.533C>T
|
ENSP00000498322.1:p.Ala178Val
|
|
ENST00000651676.1:c.533C>T
|
ENSP00000498699.1:p.Ala178Val
|
|
ENST00000651994.1:c.*70-4771C>T
|
ENSP00000498310.1:n.*70-4771C>T
|
|
ENST00000652718.1:c.365C>T
|
ENSP00000498866.1:p.Ala122Val
|
|
ENST00000360215.2:c.533C>T
|
ENSP00000353346.1:p.Ala178Val
|
|
ENST00000496656.1:n.312C>T
|
|
|
NM_182548.3:c.533C>T
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NP_872354.1:p.Ala178Val
|
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XM_011514403.1:c.533C>T
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XP_011512705.1:p.Ala178Val
|
|
NM_182548.4:c.533C>T
MANE Select
|
NP_872354.1:p.Ala178Val
|
|