ENST00000256646.7:c.1168T>G
MANE Select
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ENSP00000256646.2:p.Cys390Gly
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ENST00000640021.1:c.388T>G
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ENSP00000492223.1:n.388T>G
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ENST00000256646.6:c.1168T>G
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ENSP00000256646.2:p.Cys390Gly
|
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ENST00000479412.2:n.1306T>G
|
|
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ENST00000579475.7:c.1051T>G
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ENSP00000477065.2:p.Cys351Gly
|
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NM_001200001.1:c.1168T>G
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NP_001186930.1:p.Cys390Gly
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NM_024408.3:c.1168T>G
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NP_077719.2:p.Cys390Gly
|
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XM_005270901.2:c.1051T>G
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XP_005270958.1:p.Cys351Gly
|
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XM_011541519.1:c.1156T>G
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XP_011539821.1:p.Cys386Gly
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XM_011541520.1:c.1051T>G
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XP_011539822.1:p.Cys351Gly
|
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NM_024408.4:c.1168T>G
MANE Select
|
NP_077719.2:p.Cys390Gly
|
|
NM_001200001.2:c.1168T>G
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NP_001186930.1:p.Cys390Gly
|
|