ENST00000477226.6:n.669G>A
|
|
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ENST00000683013.1:n.583G>A
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|
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ENST00000373960.4:c.1195G>A
MANE Select
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ENSP00000363071.3:p.Asp399Asn
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|
ENST00000373960.3:c.1195G>A
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ENSP00000363071.3:p.Asp399Asn
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ENST00000477226.5:n.667G>A
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|
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ENST00000492726.1:n.590G>A
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NM_001927.3:c.1195G>A , LRG_380t1:c.1195G>A
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NP_001918.3:p.Asp399Asn
|
|
NM_001927.4:c.1195G>A
MANE Select
|
NP_001918.3:p.Asp399Asn
|
|
NM_001382708.1:c.1192G>A
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NP_001369637.1:p.Asp398Asn
|
|
NM_001382709.1:c.763G>A
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NP_001369638.1:p.Asp255Asn
|
|
NM_001382710.1:c.1126G>A
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NP_001369639.1:p.Asp376Asn
|
|
NM_001382711.1:c.1174G>A
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NP_001369640.1:p.Asp392Asn
|
|
NM_001382712.1:c.1195G>A
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NP_001369641.1:p.Asp399Asn
|
|
NM_001382713.1:c.925G>A
|
NP_001369642.1:p.Asp309Asn
|
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