ENST00000268314.9:c.955G>T
MANE Select
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ENSP00000268314.4:p.Gly319Cys
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ENST00000268314.8:c.955G>T
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ENSP00000268314.4:p.Gly319Cys
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ENST00000408912.7:c.1240G>T
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ENSP00000386125.3:p.Gly414Cys
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ENST00000457010.6:c.955G>T
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ENSP00000399561.2:p.Gly319Cys
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ENST00000538189.5:c.463G>T
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ENSP00000443995.2:p.Gly155Cys
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ENST00000563544.5:c.955G>T
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ENSP00000456877.1:p.Gly319Cys
|
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ENST00000564900.1:c.213-270G>T
|
|
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NM_001105247.1:c.955G>T
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NP_001098717.1:p.Gly319Cys
|
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NM_001288767.1:c.1240G>T
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NP_001275696.1:p.Gly414Cys
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NM_001301820.1:c.1051G>T
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NP_001288749.1:p.Gly351Cys
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NM_024742.2:c.955G>T
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NP_079018.1:p.Gly319Cys
|
|
XM_006721091.1:c.1051G>T
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XP_006721154.1:p.Gly351Cys
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XM_006721091.3:c.1051G>T
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XP_006721154.1:p.Gly351Cys
|
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XM_024450448.1:c.1051G>T
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XP_024306216.1:p.Gly351Cys
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XM_024450449.1:c.1051G>T
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XP_024306217.1:p.Gly351Cys
|
|
NM_001105247.2:c.955G>T
MANE Select
|
NP_001098717.1:p.Gly319Cys
|
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NM_001288767.2:c.1240G>T
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NP_001275696.1:p.Gly414Cys
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