ENST00000296684.10:c.195T>A
MANE Select
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ENSP00000296684.5:p.Thr65=
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ENST00000296684.9:c.195T>A
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ENSP00000296684.5:p.Thr65=
|
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ENST00000502423.5:c.*62T>A
|
ENSP00000422177.1:n.*62T>A
|
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ENST00000506765.1:c.183T>A
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ENSP00000424570.1:p.Thr61=
|
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ENST00000506974.5:c.367T>A
|
ENSP00000425967.1:p.Trp123Arg
|
|
ENST00000507026.5:c.*169T>A
|
ENSP00000424993.1:n.*169T>A
|
|
ENST00000509443.1:n.56T>A
|
|
|
NM_002495.2:c.195T>A
|
NP_002486.1:p.Thr65=
|
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XM_005248525.3:c.195T>A
|
XP_005248582.1:p.Thr65=
|
|
XM_011543415.1:c.21T>A
|
XP_011541717.1:p.Thr7=
|
|
NM_001318051.1:c.195T>A
|
NP_001304980.1:p.Thr65=
|
|
NM_002495.3:c.195T>A
|
NP_002486.1:p.Thr65=
|
|
NR_134473.1:n.397T>A
|
|
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NR_134474.1:n.314T>A
|
|
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NR_134475.1:n.349T>A
|
|
|
NM_002495.4:c.195T>A
MANE Select
|
NP_002486.1:p.Thr65=
|
|
NM_001318051.2:c.195T>A
|
NP_001304980.1:p.Thr65=
|
|
NR_134473.2:n.391T>A
|
|
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NR_134474.2:n.308T>A
|
|
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NR_134475.2:n.343T>A
|
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