ENST00000267845.8:c.1767T>A
MANE Select
|
ENSP00000267845.3:p.Ser589Arg
|
|
ENST00000267845.7:c.1767T>A
|
ENSP00000267845.3:p.Ser589Arg
|
|
ENST00000543581.5:c.1668T>A
|
ENSP00000440252.1:p.Ser556Arg
|
|
ENST00000559816.1:n.1511T>A
|
|
|
NM_001306146.1:c.1668T>A
|
NP_001293075.1:p.Ser556Arg
|
|
NM_002112.3:c.1767T>A
|
NP_002103.2:p.Ser589Arg
|
|
XM_011521479.1:c.1530T>A
|
XP_011519781.1:p.Ser510Arg
|
|
XM_011521480.1:c.1335T>A
|
XP_011519782.1:p.Ser445Arg
|
|
XM_017022094.1:c.1872T>A
|
XP_016877583.1:p.Ser624Arg
|
|
XM_017022095.1:c.1773T>A
|
XP_016877584.1:p.Ser591Arg
|
|
XM_017022096.1:c.1644T>A
|
XP_016877585.1:p.Ser548Arg
|
|
XM_017022097.1:c.1635T>A
|
XP_016877586.1:p.Ser545Arg
|
|
XM_017022098.1:c.1440T>A
|
XP_016877587.1:p.Ser480Arg
|
|
NM_002112.4:c.1767T>A
MANE Select
|
NP_002103.2:p.Ser589Arg
|
|
NM_001306146.2:c.1668T>A
|
NP_001293075.1:p.Ser556Arg
|
|