ENST00000355832.10:c.3710A>G
MANE Select
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ENSP00000348089.5:p.Glu1237Gly
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ENST00000679552.1:n.781A>G
|
|
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ENST00000679871.1:n.856A>G
|
|
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ENST00000679974.1:n.759A>G
|
|
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ENST00000681632.1:n.5113A>G
|
|
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ENST00000681659.1:c.3551A>G
|
ENSP00000505631.1:p.Glu1184Gly
|
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ENST00000355832.9:c.3710A>G
|
ENSP00000348089.5:p.Glu1237Gly
|
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ENST00000465653.1:n.32A>G
|
|
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ENST00000623073.3:c.*2006A>G
|
ENSP00000485650.1:n.*2006A>G
|
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ENST00000623115.3:c.1820A>G
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ENSP00000485321.1:p.Glu607Gly
|
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ENST00000624341.3:c.1542A>G
|
|
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NM_000124.3:c.3710A>G
|
NP_000115.1:p.Glu1237Gly
|
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XR_945953.1:n.243-1315T>C
|
|
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NM_001346440.1:c.3710A>G
|
NP_001333369.1:p.Glu1237Gly
|
|
NM_000124.4:c.3710A>G
MANE Select
|
NP_000115.1:p.Glu1237Gly
|
|
NM_001346440.2:c.3710A>G
|
NP_001333369.1:p.Glu1237Gly
|
|