ENST00000309424.8:c.162A>G
MANE Select
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ENSP00000310966.3:p.Glu54=
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ENST00000309424.7:c.162A>G
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ENSP00000310966.3:p.Glu54=
|
|
ENST00000589804.1:c.168A>G
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ENSP00000465099.1:p.Glu56=
|
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ENST00000590794.1:c.20+515A>G
|
|
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ENST00000592852.1:c.-373A>G
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ENSP00000467771.1:n.-373A>G
|
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NM_001297590.1:c.168A>G
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NP_001284519.1:p.Glu56=
|
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NM_012099.1:c.162A>G
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NP_036231.1:p.Glu54=
|
|
NM_001297590.2:c.168A>G
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NP_001284519.1:p.Glu56=
|
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NM_012099.2:c.162A>G
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NP_036231.1:p.Glu54=
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NM_001297590.3:c.168A>G
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NP_001284519.1:p.Glu56=
|
|
NM_012099.3:c.162A>G
MANE Select
|
NP_036231.1:p.Glu54=
|
|