ENST00000409155.8:c.905A>C
MANE Select
|
ENSP00000386284.3:p.Glu302Ala
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ENST00000409155.7:c.905A>C
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ENSP00000386284.3:p.Glu302Ala
|
|
ENST00000482847.5:n.1178A>C
|
|
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NM_000031.5:c.905A>C
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NP_000022.3:p.Glu302Ala
|
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XM_005251799.1:c.992A>C
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XP_005251856.1:p.Glu331Ala
|
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XM_011518363.1:c.1031A>C
|
XP_011516665.1:p.Glu344Ala
|
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XM_011518364.1:c.932A>C
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XP_011516666.1:p.Glu311Ala
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NM_001003945.2:c.992A>C
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NP_001003945.1:p.Glu331Ala
|
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NM_001317745.1:c.881A>C
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NP_001304674.1:p.Glu294Ala
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XM_011518364.2:c.932A>C
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XP_011516666.1:p.Glu311Ala
|
|
XM_024447449.1:c.992A>C
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XP_024303217.1:p.Glu331Ala
|
|
NM_000031.6:c.905A>C
MANE Select
|
NP_000022.3:p.Glu302Ala
|
|
NM_001003945.3:c.992A>C
|
NP_001003945.1:p.Glu331Ala
|
|
NM_001317745.2:c.881A>C
|
NP_001304674.1:p.Glu294Ala
|
|