ENST00000296684.10:c.410T>G
MANE Select
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ENSP00000296684.5:p.Phe137Cys
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|
ENST00000296684.9:c.410T>G
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ENSP00000296684.5:p.Phe137Cys
|
|
ENST00000502423.5:c.*277T>G
|
ENSP00000422177.1:n.*277T>G
|
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ENST00000506765.1:c.338+12205T>G
|
ENSP00000424570.1:n.338+12205T>G
|
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ENST00000506974.5:c.*186T>G
|
ENSP00000425967.1:n.*186T>G
|
|
ENST00000507026.5:c.*384T>G
|
ENSP00000424993.1:n.*384T>G
|
|
ENST00000509443.1:n.271T>G
|
|
|
NM_002495.2:c.410T>G
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NP_002486.1:p.Phe137Cys
|
|
XM_005248525.3:c.350+12205T>G
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XP_005248582.1:n.350+12205T>G
|
|
XM_011543415.1:c.236T>G
|
XP_011541717.1:p.Phe79Cys
|
|
NM_001318051.1:c.350+12205T>G
|
NP_001304980.1:n.350+12205T>G
|
|
NM_002495.3:c.410T>G
|
NP_002486.1:p.Phe137Cys
|
|
NR_134473.1:n.612T>G
|
|
|
NR_134474.1:n.529T>G
|
|
|
NR_134475.1:n.564T>G
|
|
|
NM_002495.4:c.410T>G
MANE Select
|
NP_002486.1:p.Phe137Cys
|
|
NM_001318051.2:c.350+12205T>G
|
NP_001304980.1:n.350+12205T>G
|
|
NR_134473.2:n.606T>G
|
|
|
NR_134474.2:n.523T>G
|
|
|
NR_134475.2:n.558T>G
|
|
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