ENST00000267845.8:c.1841T>A
MANE Select
|
ENSP00000267845.3:p.Ile614Asn
|
|
ENST00000267845.7:c.1841T>A
|
ENSP00000267845.3:p.Ile614Asn
|
|
ENST00000543581.5:c.1742T>A
|
ENSP00000440252.1:p.Ile581Asn
|
|
ENST00000559816.1:n.1585T>A
|
|
|
NM_001306146.1:c.1742T>A
|
NP_001293075.1:p.Ile581Asn
|
|
NM_002112.3:c.1841T>A
|
NP_002103.2:p.Ile614Asn
|
|
XM_011521479.1:c.1604T>A
|
XP_011519781.1:p.Ile535Asn
|
|
XM_011521480.1:c.1409T>A
|
XP_011519782.1:p.Ile470Asn
|
|
XM_017022094.1:c.1946T>A
|
XP_016877583.1:p.Ile649Asn
|
|
XM_017022095.1:c.1847T>A
|
XP_016877584.1:p.Ile616Asn
|
|
XM_017022096.1:c.1718T>A
|
XP_016877585.1:p.Ile573Asn
|
|
XM_017022097.1:c.1709T>A
|
XP_016877586.1:p.Ile570Asn
|
|
XM_017022098.1:c.1514T>A
|
XP_016877587.1:p.Ile505Asn
|
|
NM_002112.4:c.1841T>A
MANE Select
|
NP_002103.2:p.Ile614Asn
|
|
NM_001306146.2:c.1742T>A
|
NP_001293075.1:p.Ile581Asn
|
|