ENST00000324856.13:c.5237A>G
MANE Select
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ENSP00000320485.7:p.Asp1746Gly
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ENST00000374152.7:c.4088A>G
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ENSP00000363267.2:p.Asp1363Gly
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ENST00000430799.7:c.4085A>G
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ENSP00000390317.3:p.Asp1362Gly
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ENST00000466382.2:c.654A>G
|
|
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ENST00000636219.1:c.4091A>G
|
ENSP00000489842.1:p.Asp1364Gly
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ENST00000637788.1:n.1037A>G
|
|
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ENST00000324856.11:c.5237A>G
|
ENSP00000320485.7:p.Asp1746Gly
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ENST00000374152.6:c.4088A>G
|
ENSP00000363267.2:p.Asp1363Gly
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ENST00000430799.6:c.1926A>G
|
|
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ENST00000457599.6:c.4586A>G
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ENSP00000387636.2:p.Asp1529Gly
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ENST00000466382.1:c.654A>G
|
|
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ENST00000532781.1:c.735A>G
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NM_006015.4:c.5237A>G , LRG_875t1:c.5237A>G
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NP_006006.3:p.Asp1746Gly
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NM_139135.2:c.4586A>G
|
NP_624361.1:p.Asp1529Gly
|
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NM_006015.5:c.5237A>G
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NP_006006.3:p.Asp1746Gly
|
|
NM_139135.3:c.4586A>G
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NP_624361.1:p.Asp1529Gly
|
|
NM_006015.6:c.5237A>G
MANE Select
|
NP_006006.3:p.Asp1746Gly
|
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NM_139135.4:c.4586A>G
|
NP_624361.1:p.Asp1529Gly
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