ENST00000261819.8:c.1851G>C
MANE Select
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ENSP00000261819.3:p.Gln617His
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ENST00000261819.7:c.1851G>C
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ENSP00000261819.3:p.Gln617His
|
|
ENST00000441917.6:c.1515G>C
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ENSP00000415061.2:p.Gln505His
|
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ENST00000534976.5:n.2583G>C
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|
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ENST00000535482.1:c.849G>C
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ENSP00000438754.1:p.Gln283His
|
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ENST00000535641.5:n.2062G>C
|
|
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ENST00000539079.5:c.1175G>C
|
|
|
ENST00000541887.5:c.1812G>C
|
ENSP00000439875.1:p.Gln604His
|
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ENST00000544314.5:n.969G>C
|
|
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ENST00000545218.5:n.1021G>C
|
|
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NM_001137559.1:c.1515G>C
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NP_001131031.1:p.Gln505His
|
|
NM_016237.4:c.1851G>C
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NP_057321.2:p.Gln617His
|
|
XM_005253900.2:c.1812G>C
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XP_005253957.1:p.Gln604His
|
|
XM_006719449.1:c.657G>C
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XP_006719512.1:p.Gln219His
|
|
NM_001330489.1:c.1812G>C
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NP_001317418.1:p.Gln604His
|
|
XM_017019423.2:c.657G>C
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XP_016874912.1:p.Gln219His
|
|
XM_017019424.2:c.657G>C
|
XP_016874913.1:p.Gln219His
|
|
NM_016237.5:c.1851G>C
MANE Select
|
NP_057321.2:p.Gln617His
|
|
NM_001330489.2:c.1812G>C
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NP_001317418.1:p.Gln604His
|
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