ENST00000420175.3:c.531T>C
MANE Select
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ENSP00000391137.2:p.Ala177=
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ENST00000275838.5:c.531T>C
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ENSP00000275838.1:p.Ala177=
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ENST00000377867.7:c.486T>C
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ENSP00000367098.3:p.Ala162=
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ENST00000420175.2:c.531T>C
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ENSP00000391137.2:p.Ala177=
|
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NM_001142459.1:c.531T>C
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NP_001135931.2:p.Ala177=
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NM_001142460.1:c.531T>C
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NP_001135932.2:p.Ala177=
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NM_080871.3:c.486T>C
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NP_543147.2:p.Ala162=
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XM_005249949.3:c.666T>C
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XP_005250006.1:p.Ala222=
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NM_001142459.2:c.531T>C
MANE Select
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NP_001135931.2:p.Ala177=
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NM_080871.4:c.486T>C
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NP_543147.2:p.Ala162=
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