ENST00000267845.8:c.1762A>G
MANE Select
|
ENSP00000267845.3:p.Asn588Asp
|
|
ENST00000267845.7:c.1762A>G
|
ENSP00000267845.3:p.Asn588Asp
|
|
ENST00000543581.5:c.1663A>G
|
ENSP00000440252.1:p.Asn555Asp
|
|
ENST00000559816.1:n.1506A>G
|
|
|
NM_001306146.1:c.1663A>G
|
NP_001293075.1:p.Asn555Asp
|
|
NM_002112.3:c.1762A>G
|
NP_002103.2:p.Asn588Asp
|
|
XM_011521479.1:c.1525A>G
|
XP_011519781.1:p.Asn509Asp
|
|
XM_011521480.1:c.1330A>G
|
XP_011519782.1:p.Asn444Asp
|
|
XM_017022094.1:c.1867A>G
|
XP_016877583.1:p.Asn623Asp
|
|
XM_017022095.1:c.1768A>G
|
XP_016877584.1:p.Asn590Asp
|
|
XM_017022096.1:c.1639A>G
|
XP_016877585.1:p.Asn547Asp
|
|
XM_017022097.1:c.1630A>G
|
XP_016877586.1:p.Asn544Asp
|
|
XM_017022098.1:c.1435A>G
|
XP_016877587.1:p.Asn479Asp
|
|
NM_002112.4:c.1762A>G
MANE Select
|
NP_002103.2:p.Asn588Asp
|
|
NM_001306146.2:c.1663A>G
|
NP_001293075.1:p.Asn555Asp
|
|