ENST00000684241.1:n.1848A>G
|
|
|
ENST00000262186.10:c.1015A>G
MANE Select
|
ENSP00000262186.5:p.Asn339Asp
|
|
ENST00000262186.9:c.1015A>G
|
ENSP00000262186.5:p.Asn339Asp
|
|
ENST00000430723.4:c.667A>G
|
ENSP00000387657.4:p.Asn223Asp
|
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ENST00000532957.5:n.1238A>G
|
|
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NM_000238.3:c.1015A>G , LRG_288t1:c.1015A>G
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NP_000229.1:p.Asn339Asp
|
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NM_172056.2:c.1015A>G , LRG_288t2:c.1015A>G
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NP_742053.1:p.Asn339Asp
|
|
XM_011516185.1:c.715A>G
|
XP_011514487.1:p.Asn239Asp
|
|
XM_011516186.1:c.1015A>G
|
XP_011514488.1:p.Asn339Asp
|
|
XM_011516185.2:c.715A>G
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XP_011514487.1:p.Asn239Asp
|
|
XM_011516186.3:c.1015A>G
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XP_011514488.1:p.Asn339Asp
|
|
XM_017012195.1:c.865A>G
|
XP_016867684.1:p.Asn289Asp
|
|
XM_017012196.1:c.838A>G
|
XP_016867685.1:p.Asn280Asp
|
|
NM_000238.4:c.1015A>G
MANE Select
|
NP_000229.1:p.Asn339Asp
|
|