ENST00000267845.8:c.1762A>T
MANE Select
|
ENSP00000267845.3:p.Asn588Tyr
|
|
ENST00000267845.7:c.1762A>T
|
ENSP00000267845.3:p.Asn588Tyr
|
|
ENST00000543581.5:c.1663A>T
|
ENSP00000440252.1:p.Asn555Tyr
|
|
ENST00000559816.1:n.1506A>T
|
|
|
NM_001306146.1:c.1663A>T
|
NP_001293075.1:p.Asn555Tyr
|
|
NM_002112.3:c.1762A>T
|
NP_002103.2:p.Asn588Tyr
|
|
XM_011521479.1:c.1525A>T
|
XP_011519781.1:p.Asn509Tyr
|
|
XM_011521480.1:c.1330A>T
|
XP_011519782.1:p.Asn444Tyr
|
|
XM_017022094.1:c.1867A>T
|
XP_016877583.1:p.Asn623Tyr
|
|
XM_017022095.1:c.1768A>T
|
XP_016877584.1:p.Asn590Tyr
|
|
XM_017022096.1:c.1639A>T
|
XP_016877585.1:p.Asn547Tyr
|
|
XM_017022097.1:c.1630A>T
|
XP_016877586.1:p.Asn544Tyr
|
|
XM_017022098.1:c.1435A>T
|
XP_016877587.1:p.Asn479Tyr
|
|
NM_002112.4:c.1762A>T
MANE Select
|
NP_002103.2:p.Asn588Tyr
|
|
NM_001306146.2:c.1663A>T
|
NP_001293075.1:p.Asn555Tyr
|
|