ENST00000252288.8:c.444G>C
MANE Select
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ENSP00000252288.1:p.Gln148His
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ENST00000447102.8:c.444G>C
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ENSP00000403536.2:p.Gln148His
|
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ENST00000591788.3:c.127G>C
|
|
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ENST00000640164.1:n.277G>C
|
|
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ENST00000640762.1:c.375G>C
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ENSP00000492031.1:p.Gln125His
|
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ENST00000252288.6:c.444G>C
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ENSP00000252288.1:p.Gln148His
|
|
ENST00000447102.7:c.444G>C
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ENSP00000403536.2:p.Gln148His
|
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ENST00000591788.2:c.129G>C
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ENSP00000466341.2:p.Gln43His
|
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NM_000156.5:c.444G>C
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NP_000147.1:p.Gln148His
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NM_138924.2:c.444G>C
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NP_620279.1:p.Gln148His
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NM_000156.6:c.444G>C
MANE Select
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NP_000147.1:p.Gln148His
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NM_138924.3:c.444G>C
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NP_620279.1:p.Gln148His
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