ENST00000267845.8:c.1763A>G
MANE Select
|
ENSP00000267845.3:p.Asn588Ser
|
|
ENST00000267845.7:c.1763A>G
|
ENSP00000267845.3:p.Asn588Ser
|
|
ENST00000543581.5:c.1664A>G
|
ENSP00000440252.1:p.Asn555Ser
|
|
ENST00000559816.1:n.1507A>G
|
|
|
NM_001306146.1:c.1664A>G
|
NP_001293075.1:p.Asn555Ser
|
|
NM_002112.3:c.1763A>G
|
NP_002103.2:p.Asn588Ser
|
|
XM_011521479.1:c.1526A>G
|
XP_011519781.1:p.Asn509Ser
|
|
XM_011521480.1:c.1331A>G
|
XP_011519782.1:p.Asn444Ser
|
|
XM_017022094.1:c.1868A>G
|
XP_016877583.1:p.Asn623Ser
|
|
XM_017022095.1:c.1769A>G
|
XP_016877584.1:p.Asn590Ser
|
|
XM_017022096.1:c.1640A>G
|
XP_016877585.1:p.Asn547Ser
|
|
XM_017022097.1:c.1631A>G
|
XP_016877586.1:p.Asn544Ser
|
|
XM_017022098.1:c.1436A>G
|
XP_016877587.1:p.Asn479Ser
|
|
NM_002112.4:c.1763A>G
MANE Select
|
NP_002103.2:p.Asn588Ser
|
|
NM_001306146.2:c.1664A>G
|
NP_001293075.1:p.Asn555Ser
|
|