ENST00000221930.6:c.649T>G
MANE Select
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ENSP00000221930.4:p.Phe217Val
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ENST00000600196.2:c.649T>G
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ENSP00000504008.1:p.Phe217Val
|
|
ENST00000677934.1:c.634+2514T>G
|
ENSP00000504769.1:n.634+2514T>G
|
|
ENST00000221930.5:c.649T>G
|
ENSP00000221930.4:p.Phe217Val
|
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ENST00000597453.1:n.180T>G
|
|
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ENST00000600196.1:n.109T>G
|
|
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NM_000660.5:c.649T>G
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NP_000651.3:p.Phe217Val
|
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XM_011527242.1:c.649T>G
|
XP_011525544.1:p.Phe217Val
|
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NM_000660.6:c.649T>G
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NP_000651.3:p.Phe217Val
|
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XM_011527242.2:c.649T>G
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XP_011525544.1:p.Phe217Val
|
|
NM_000660.7:c.649T>G
MANE Select
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NP_000651.3:p.Phe217Val
|
|