ENST00000376810.6:c.501C>T
MANE Select
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ENSP00000366006.5:p.Gly167=
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ENST00000376804.2:c.501C>T
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ENSP00000366000.1:p.Gly167=
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|
ENST00000376810.5:c.501C>T
|
ENSP00000366006.5:p.Gly167=
|
|
ENST00000483738.1:c.99C>T
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ENSP00000473453.1:p.Gly33=
|
|
ENST00000486588.6:c.144C>T
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ENSP00000473612.1:p.Gly48=
|
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NM_013319.2:c.501C>T
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NP_037451.1:p.Gly167=
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XM_006710590.2:c.501C>T
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XP_006710653.1:p.Gly167=
|
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XM_011541304.1:c.501C>T
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XP_011539606.1:p.Gly167=
|
|
XR_946616.1:n.835C>T
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|
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NM_001330349.1:c.501C>T
|
NP_001317278.1:p.Gly167=
|
|
NM_001330350.1:c.501C>T
|
NP_001317279.1:p.Gly167=
|
|
XR_946616.3:n.835C>T
|
|
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NM_001330349.2:c.501C>T
|
NP_001317278.1:p.Gly167=
|
|
NM_001330350.2:c.501C>T
|
NP_001317279.1:p.Gly167=
|
|
NM_013319.3:c.501C>T
MANE Select
|
NP_037451.1:p.Gly167=
|
|