ENST00000267845.8:c.1766G>A
MANE Select
|
ENSP00000267845.3:p.Ser589Asn
|
|
ENST00000267845.7:c.1766G>A
|
ENSP00000267845.3:p.Ser589Asn
|
|
ENST00000543581.5:c.1667G>A
|
ENSP00000440252.1:p.Ser556Asn
|
|
ENST00000559816.1:n.1510G>A
|
|
|
NM_001306146.1:c.1667G>A
|
NP_001293075.1:p.Ser556Asn
|
|
NM_002112.3:c.1766G>A
|
NP_002103.2:p.Ser589Asn
|
|
XM_011521479.1:c.1529G>A
|
XP_011519781.1:p.Ser510Asn
|
|
XM_011521480.1:c.1334G>A
|
XP_011519782.1:p.Ser445Asn
|
|
XM_017022094.1:c.1871G>A
|
XP_016877583.1:p.Ser624Asn
|
|
XM_017022095.1:c.1772G>A
|
XP_016877584.1:p.Ser591Asn
|
|
XM_017022096.1:c.1643G>A
|
XP_016877585.1:p.Ser548Asn
|
|
XM_017022097.1:c.1634G>A
|
XP_016877586.1:p.Ser545Asn
|
|
XM_017022098.1:c.1439G>A
|
XP_016877587.1:p.Ser480Asn
|
|
NM_002112.4:c.1766G>A
MANE Select
|
NP_002103.2:p.Ser589Asn
|
|
NM_001306146.2:c.1667G>A
|
NP_001293075.1:p.Ser556Asn
|
|