ENST00000367698.4:c.1306G>A
MANE Select
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ENSP00000356671.3:p.Ala436Thr
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ENST00000367698.3:c.1306G>A
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ENSP00000356671.3:p.Ala436Thr
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ENST00000617423.4:c.691G>A
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ENSP00000478688.1:p.Ala231Thr
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NM_000488.3:c.1306G>A , LRG_577t1:c.1306G>A
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NP_000479.1:p.Ala436Thr
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XM_005245198.2:c.1162G>A
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XP_005245255.1:p.Ala388Thr
|
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NM_001365052.1:c.1162G>A
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NP_001351981.1:p.Ala388Thr
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NM_000488.4:c.1306G>A
MANE Select
|
NP_000479.1:p.Ala436Thr
|
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NM_001365052.2:c.1162G>A
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NP_001351981.1:p.Ala388Thr
|
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NM_001386302.1:c.1429G>A
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NP_001373231.1:p.Ala477Thr
|
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NM_001386303.1:c.1387G>A
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NP_001373232.1:p.Ala463Thr
|
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NM_001386304.1:c.1285G>A
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NP_001373233.1:p.Ala429Thr
|
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NM_001386305.1:c.1249G>A
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NP_001373234.1:p.Ala417Thr
|
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NM_001386306.1:c.1090G>A
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NP_001373235.1:p.Ala364Thr
|
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