ENST00000420175.3:c.451G>A
MANE Select
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ENSP00000391137.2:p.Ala151Thr
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ENST00000275838.5:c.451G>A
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ENSP00000275838.1:p.Ala151Thr
|
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ENST00000377867.7:c.406G>A
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ENSP00000367098.3:p.Ala136Thr
|
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ENST00000420175.2:c.451G>A
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ENSP00000391137.2:p.Ala151Thr
|
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NM_001142459.1:c.451G>A
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NP_001135931.2:p.Ala151Thr
|
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NM_001142460.1:c.451G>A
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NP_001135932.2:p.Ala151Thr
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NM_080871.3:c.406G>A
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NP_543147.2:p.Ala136Thr
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XM_005249949.3:c.586G>A
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XP_005250006.1:p.Ala196Thr
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NM_001142459.2:c.451G>A
MANE Select
|
NP_001135931.2:p.Ala151Thr
|
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NM_080871.4:c.406G>A
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NP_543147.2:p.Ala136Thr
|
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