ENST00000367698.4:c.829G>A
MANE Select
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ENSP00000356671.3:p.Glu277Lys
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ENST00000367698.3:c.829G>A
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ENSP00000356671.3:p.Glu277Lys
|
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ENST00000487183.1:n.480G>A
|
|
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ENST00000617423.4:c.559+1988G>A
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ENSP00000478688.1:n.559+1988G>A
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NM_000488.3:c.829G>A , LRG_577t1:c.829G>A
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NP_000479.1:p.Glu277Lys
|
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XM_005245198.2:c.685G>A
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XP_005245255.1:p.Glu229Lys
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NM_001365052.1:c.685G>A
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NP_001351981.1:p.Glu229Lys
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NM_000488.4:c.829G>A
MANE Select
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NP_000479.1:p.Glu277Lys
|
|
NM_001365052.2:c.685G>A
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NP_001351981.1:p.Glu229Lys
|
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NM_001386302.1:c.952G>A
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NP_001373231.1:p.Glu318Lys
|
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NM_001386303.1:c.910G>A
|
NP_001373232.1:p.Glu304Lys
|
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NM_001386304.1:c.808G>A
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NP_001373233.1:p.Glu270Lys
|
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NM_001386305.1:c.772G>A
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NP_001373234.1:p.Glu258Lys
|
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NM_001386306.1:c.613G>A
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NP_001373235.1:p.Glu205Lys
|
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