ENST00000380036.10:c.2725A>G
MANE Select
|
ENSP00000369375.4:p.Asn909Asp
|
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ENST00000380036.8:c.2725A>G
|
ENSP00000369375.4:p.Asn909Asp
|
|
ENST00000406359.8:c.2596A>G
|
ENSP00000383977.4:p.Asn866Asp
|
|
ENST00000519097.5:c.2281A>G
|
ENSP00000430686.1:p.Asn761Asp
|
|
ENST00000615002.4:c.*1226A>G
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ENSP00000480251.1:n.*1226A>G
|
|
NM_000459.4:c.2725A>G
|
NP_000450.2:p.Asn909Asp
|
|
NM_001290077.1:c.2596A>G
|
NP_001277006.1:p.Asn866Asp
|
|
NM_001290078.1:c.2281A>G
|
NP_001277007.1:p.Asn761Asp
|
|
XM_005251561.1:c.2722A>G
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XP_005251618.1:p.Asn908Asp
|
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XM_005251563.1:c.2593A>G
|
XP_005251620.1:p.Asn865Asp
|
|
XM_005251561.2:c.2722A>G
|
XP_005251618.1:p.Asn908Asp
|
|
XM_005251563.2:c.2593A>G
|
XP_005251620.1:p.Asn865Asp
|
|
NM_000459.5:c.2725A>G
MANE Select
|
NP_000450.3:p.Asn909Asp
|
|
NM_001375475.1:c.2722A>G
|
NP_001362404.1:p.Asn908Asp
|
|
NM_001375476.1:c.2593A>G
|
NP_001362405.1:p.Asn865Asp
|
|