ENST00000360215.3:c.645A>T
MANE Select
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ENSP00000353346.1:p.Gly215=
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ENST00000496656.2:n.424A>T
|
|
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ENST00000651132.1:c.645A>T
|
ENSP00000498322.1:p.Gly215=
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ENST00000651676.1:c.645A>T
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ENSP00000498699.1:p.Gly215=
|
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ENST00000651994.1:c.*70-4659A>T
|
ENSP00000498310.1:n.*70-4659A>T
|
|
ENST00000652718.1:c.477A>T
|
ENSP00000498866.1:p.Gly159=
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|
ENST00000360215.2:c.645A>T
|
ENSP00000353346.1:p.Gly215=
|
|
ENST00000496656.1:n.424A>T
|
|
|
NM_182548.3:c.645A>T
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NP_872354.1:p.Gly215=
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XM_011514403.1:c.645A>T
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XP_011512705.1:p.Gly215=
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NM_182548.4:c.645A>T
MANE Select
|
NP_872354.1:p.Gly215=
|
|