ENST00000267845.8:c.1712G>C
MANE Select
|
ENSP00000267845.3:p.Ser571Thr
|
|
ENST00000267845.7:c.1712G>C
|
ENSP00000267845.3:p.Ser571Thr
|
|
ENST00000543581.5:c.1613G>C
|
ENSP00000440252.1:p.Ser538Thr
|
|
ENST00000559816.1:n.1456G>C
|
|
|
NM_001306146.1:c.1613G>C
|
NP_001293075.1:p.Ser538Thr
|
|
NM_002112.3:c.1712G>C
|
NP_002103.2:p.Ser571Thr
|
|
XM_011521479.1:c.1475G>C
|
XP_011519781.1:p.Ser492Thr
|
|
XM_011521480.1:c.1280G>C
|
XP_011519782.1:p.Ser427Thr
|
|
XM_017022094.1:c.1817G>C
|
XP_016877583.1:p.Ser606Thr
|
|
XM_017022095.1:c.1718G>C
|
XP_016877584.1:p.Ser573Thr
|
|
XM_017022096.1:c.1589G>C
|
XP_016877585.1:p.Ser530Thr
|
|
XM_017022097.1:c.1580G>C
|
XP_016877586.1:p.Ser527Thr
|
|
XM_017022098.1:c.1385G>C
|
XP_016877587.1:p.Ser462Thr
|
|
NM_002112.4:c.1712G>C
MANE Select
|
NP_002103.2:p.Ser571Thr
|
|
NM_001306146.2:c.1613G>C
|
NP_001293075.1:p.Ser538Thr
|
|