ENST00000644719.2:c.770T>A
MANE Select
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ENSP00000496625.1:p.Met257Lys
|
|
ENST00000418967.6:c.770T>A
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ENSP00000408860.2:p.Met257Lys
|
|
ENST00000435122.3:c.680T>A
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ENSP00000415043.2:p.Met227Lys
|
|
ENST00000479074.5:n.828T>A
|
|
|
ENST00000479730.5:n.886T>A
|
|
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ENST00000483041.5:n.939T>A
|
|
|
ENST00000486063.5:n.918+201T>A
|
|
|
NM_000500.7:c.770T>A
|
NP_000491.4:p.Met257Lys
|
|
NM_001128590.3:c.680T>A
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NP_001122062.3:p.Met227Lys
|
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XM_011514314.1:c.365T>A
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XP_011512616.1:p.Met122Lys
|
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NM_000500.9:c.770T>A
MANE Select
|
NP_000491.4:p.Met257Lys
|
|
NM_001368143.1:c.365T>A
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NP_001355072.1:p.Met122Lys
|
|
NM_001368144.1:c.365T>A
|
NP_001355073.1:p.Met122Lys
|
|
NM_001128590.4:c.680T>A
|
NP_001122062.3:p.Met227Lys
|
|
NM_001368143.2:c.365T>A
|
NP_001355072.1:p.Met122Lys
|
|
NM_001368144.2:c.365T>A
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NP_001355073.1:p.Met122Lys
|
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