ENST00000267845.8:c.1825T>A
MANE Select
|
ENSP00000267845.3:p.Ser609Thr
|
|
ENST00000267845.7:c.1825T>A
|
ENSP00000267845.3:p.Ser609Thr
|
|
ENST00000543581.5:c.1726T>A
|
ENSP00000440252.1:p.Ser576Thr
|
|
ENST00000559816.1:n.1569T>A
|
|
|
NM_001306146.1:c.1726T>A
|
NP_001293075.1:p.Ser576Thr
|
|
NM_002112.3:c.1825T>A
|
NP_002103.2:p.Ser609Thr
|
|
XM_011521479.1:c.1588T>A
|
XP_011519781.1:p.Ser530Thr
|
|
XM_011521480.1:c.1393T>A
|
XP_011519782.1:p.Ser465Thr
|
|
XM_017022094.1:c.1930T>A
|
XP_016877583.1:p.Ser644Thr
|
|
XM_017022095.1:c.1831T>A
|
XP_016877584.1:p.Ser611Thr
|
|
XM_017022096.1:c.1702T>A
|
XP_016877585.1:p.Ser568Thr
|
|
XM_017022097.1:c.1693T>A
|
XP_016877586.1:p.Ser565Thr
|
|
XM_017022098.1:c.1498T>A
|
XP_016877587.1:p.Ser500Thr
|
|
NM_002112.4:c.1825T>A
MANE Select
|
NP_002103.2:p.Ser609Thr
|
|
NM_001306146.2:c.1726T>A
|
NP_001293075.1:p.Ser576Thr
|
|