ENST00000324856.13:c.5342T>G
MANE Select
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ENSP00000320485.7:p.Val1781Gly
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ENST00000374152.7:c.4193T>G
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ENSP00000363267.2:p.Val1398Gly
|
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ENST00000430799.7:c.4190T>G
|
ENSP00000390317.3:p.Val1397Gly
|
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ENST00000466382.2:c.759T>G
|
|
|
ENST00000636219.1:c.4196T>G
|
ENSP00000489842.1:p.Val1399Gly
|
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ENST00000637788.1:n.1142T>G
|
|
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ENST00000324856.11:c.5342T>G
|
ENSP00000320485.7:p.Val1781Gly
|
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ENST00000374152.6:c.4193T>G
|
ENSP00000363267.2:p.Val1398Gly
|
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ENST00000430799.6:c.2031T>G
|
|
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ENST00000457599.6:c.4691T>G
|
ENSP00000387636.2:p.Val1564Gly
|
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ENST00000466382.1:c.759T>G
|
|
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ENST00000532781.1:c.840T>G
|
|
|
NM_006015.4:c.5342T>G , LRG_875t1:c.5342T>G
|
NP_006006.3:p.Val1781Gly
|
|
NM_139135.2:c.4691T>G
|
NP_624361.1:p.Val1564Gly
|
|
NM_006015.5:c.5342T>G
|
NP_006006.3:p.Val1781Gly
|
|
NM_139135.3:c.4691T>G
|
NP_624361.1:p.Val1564Gly
|
|
NM_006015.6:c.5342T>G
MANE Select
|
NP_006006.3:p.Val1781Gly
|
|
NM_139135.4:c.4691T>G
|
NP_624361.1:p.Val1564Gly
|
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