ENST00000267845.8:c.1763A>T
MANE Select
|
ENSP00000267845.3:p.Asn588Ile
|
|
ENST00000267845.7:c.1763A>T
|
ENSP00000267845.3:p.Asn588Ile
|
|
ENST00000543581.5:c.1664A>T
|
ENSP00000440252.1:p.Asn555Ile
|
|
ENST00000559816.1:n.1507A>T
|
|
|
NM_001306146.1:c.1664A>T
|
NP_001293075.1:p.Asn555Ile
|
|
NM_002112.3:c.1763A>T
|
NP_002103.2:p.Asn588Ile
|
|
XM_011521479.1:c.1526A>T
|
XP_011519781.1:p.Asn509Ile
|
|
XM_011521480.1:c.1331A>T
|
XP_011519782.1:p.Asn444Ile
|
|
XM_017022094.1:c.1868A>T
|
XP_016877583.1:p.Asn623Ile
|
|
XM_017022095.1:c.1769A>T
|
XP_016877584.1:p.Asn590Ile
|
|
XM_017022096.1:c.1640A>T
|
XP_016877585.1:p.Asn547Ile
|
|
XM_017022097.1:c.1631A>T
|
XP_016877586.1:p.Asn544Ile
|
|
XM_017022098.1:c.1436A>T
|
XP_016877587.1:p.Asn479Ile
|
|
NM_002112.4:c.1763A>T
MANE Select
|
NP_002103.2:p.Asn588Ile
|
|
NM_001306146.2:c.1664A>T
|
NP_001293075.1:p.Asn555Ile
|
|