ENST00000375128.5:c.749A>T
MANE Select
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ENSP00000364270.5:p.Glu250Val
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ENST00000375128.4:c.749A>T
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ENSP00000364270.4:p.Glu250Val
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ENST00000462523.5:c.*185A>T
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ENSP00000433006.1:n.*185A>T
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ENST00000485042.1:n.261A>T
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NM_000380.3:c.749A>T , LRG_471t1:c.749A>T
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NP_000371.1:p.Glu250Val
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NR_027302.1:n.1097A>T
|
|
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XM_006717278.1:c.749A>T
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XP_006717341.1:p.Glu250Val
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XM_011518988.1:c.749A>T
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XP_011517290.1:p.Glu250Val
|
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XR_929839.1:n.1280A>T
|
|
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NM_001354975.1:c.623A>T
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NP_001341904.1:p.Glu208Val
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NR_149091.1:n.594A>T
|
|
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NR_149092.1:n.760A>T
|
|
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NR_149093.1:n.1286A>T
|
|
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NR_149094.1:n.1180A>T
|
|
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NM_000380.4:c.749A>T
MANE Select
|
NP_000371.1:p.Glu250Val
|
|
NM_001354975.2:c.623A>T
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NP_001341904.1:p.Glu208Val
|
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NR_027302.2:n.1028A>T
|
|
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NR_149091.2:n.525A>T
|
|
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NR_149092.2:n.691A>T
|
|
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NR_149093.2:n.1217A>T
|
|
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NR_149094.2:n.1111A>T
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