ENST00000673913.2:c.1651C>G
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ENSP00000501161.2:p.His551Asp
|
|
ENST00000710286.1:c.2008C>G
|
ENSP00000518176.1:p.His670Asp
|
|
ENST00000673903.1:c.1276C>G
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ENSP00000501257.1:p.His426Asp
|
|
ENST00000673913.1:c.391C>G
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ENSP00000501161.1:p.His131Asp
|
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ENST00000302118.5:c.1651C>G
MANE Select
|
ENSP00000303208.5:p.His551Asp
|
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ENST00000490692.1:n.2227+986C>G
|
|
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NM_174936.3:c.1651C>G , LRG_275t1:c.1651C>G
|
NP_777596.2:p.His551Asp
|
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NR_110451.1:n.1258C>G
|
|
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XM_011541193.1:c.772C>G
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XP_011539495.1:p.His258Asp
|
|
NM_174936.4:c.1651C>G
MANE Select
|
NP_777596.2:p.His551Asp
|
|
NR_110451.2:n.1258C>G
|
|
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