ENST00000426263.10:c.428A>G
MANE Select
|
ENSP00000416293.2:p.Tyr143Cys
|
|
ENST00000674765.1:c.428A>G
|
ENSP00000501811.1:p.Tyr143Cys
|
|
ENST00000675112.1:n.451A>G
|
|
|
ENST00000676254.1:n.877A>G
|
|
|
ENST00000372500.4:c.332A>G
|
ENSP00000361578.4:p.Tyr111Cys
|
|
ENST00000426263.7:c.428A>G
|
ENSP00000416293.2:p.Tyr143Cys
|
|
ENST00000439722.2:c.307A>G
|
ENSP00000395521.2:n.307A>G
|
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ENST00000475162.3:c.327A>G
|
|
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ENST00000625233.2:n.636A>G
|
|
|
ENST00000630287.2:c.428A>G
|
ENSP00000486694.1:p.Tyr143Cys
|
|
NM_006516.2:c.428A>G
|
NP_006507.2:p.Tyr143Cys
|
|
NM_006516.3:c.428A>G
|
NP_006507.2:p.Tyr143Cys
|
|
NM_006516.4:c.428A>G
MANE Select
|
NP_006507.2:p.Tyr143Cys
|
|