ENST00000651267.2:c.564G>T
MANE Select
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ENSP00000498344.1:p.Gln188His
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ENST00000215479.10:c.564G>T
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ENSP00000215479.5:p.Gln188His
|
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ENST00000651267.1:c.564G>T
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ENSP00000498344.1:p.Gln188His
|
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ENST00000215479.9:c.564G>T
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ENSP00000215479.5:p.Gln188His
|
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ENST00000383036.1:c.606G>T
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ENSP00000372505.1:p.Gln202His
|
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NM_001143.1:c.564G>T
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NP_001134.1:p.Gln188His
|
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XM_011531472.1:c.606G>T
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XP_011529774.1:p.Gln202His
|
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NM_001364814.1:c.606G>T
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NP_001351743.1:p.Gln202His
|
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NM_001143.2:c.564G>T
MANE Select
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NP_001134.1:p.Gln188His
|
|