ENST00000267845.8:c.1817A>T
MANE Select
|
ENSP00000267845.3:p.Asn606Ile
|
|
ENST00000267845.7:c.1817A>T
|
ENSP00000267845.3:p.Asn606Ile
|
|
ENST00000543581.5:c.1718A>T
|
ENSP00000440252.1:p.Asn573Ile
|
|
ENST00000559816.1:n.1561A>T
|
|
|
NM_001306146.1:c.1718A>T
|
NP_001293075.1:p.Asn573Ile
|
|
NM_002112.3:c.1817A>T
|
NP_002103.2:p.Asn606Ile
|
|
XM_011521479.1:c.1580A>T
|
XP_011519781.1:p.Asn527Ile
|
|
XM_011521480.1:c.1385A>T
|
XP_011519782.1:p.Asn462Ile
|
|
XM_017022094.1:c.1922A>T
|
XP_016877583.1:p.Asn641Ile
|
|
XM_017022095.1:c.1823A>T
|
XP_016877584.1:p.Asn608Ile
|
|
XM_017022096.1:c.1694A>T
|
XP_016877585.1:p.Asn565Ile
|
|
XM_017022097.1:c.1685A>T
|
XP_016877586.1:p.Asn562Ile
|
|
XM_017022098.1:c.1490A>T
|
XP_016877587.1:p.Asn497Ile
|
|
NM_002112.4:c.1817A>T
MANE Select
|
NP_002103.2:p.Asn606Ile
|
|
NM_001306146.2:c.1718A>T
|
NP_001293075.1:p.Asn573Ile
|
|