ENST00000644719.2:c.426G>C
MANE Select
|
ENSP00000496625.1:p.Gln142His
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ENST00000418967.6:c.426G>C
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ENSP00000408860.2:p.Gln142His
|
|
ENST00000435122.3:c.336G>C
|
ENSP00000415043.2:p.Gln112His
|
|
ENST00000462278.1:n.14G>C
|
|
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ENST00000464325.5:n.347G>C
|
|
|
ENST00000466779.5:c.*118G>C
|
ENSP00000417321.1:n.*118G>C
|
|
ENST00000466879.5:n.477G>C
|
|
|
ENST00000469053.5:c.*118G>C
|
ENSP00000418104.1:n.*118G>C
|
|
ENST00000471671.4:c.426G>C
|
ENSP00000418561.1:p.Gln142His
|
|
ENST00000478281.5:c.459G>C
|
ENSP00000419572.1:p.Gln153His
|
|
ENST00000479074.5:n.484G>C
|
|
|
ENST00000479730.5:n.581G>C
|
|
|
ENST00000483041.5:n.595G>C
|
|
|
ENST00000486063.5:n.606G>C
|
|
|
ENST00000488465.1:n.434G>C
|
|
|
NM_000500.7:c.426G>C
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NP_000491.4:p.Gln142His
|
|
NM_001128590.3:c.336G>C
|
NP_001122062.3:p.Gln112His
|
|
XM_011514314.1:c.21G>C
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XP_011512616.1:p.Gln7His
|
|
NM_000500.9:c.426G>C
MANE Select
|
NP_000491.4:p.Gln142His
|
|
NM_001368143.1:c.21G>C
|
NP_001355072.1:p.Gln7His
|
|
NM_001368144.1:c.21G>C
|
NP_001355073.1:p.Gln7His
|
|
NM_001128590.4:c.336G>C
|
NP_001122062.3:p.Gln112His
|
|
NM_001368143.2:c.21G>C
|
NP_001355072.1:p.Gln7His
|
|
NM_001368144.2:c.21G>C
|
NP_001355073.1:p.Gln7His
|
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