ENST00000267845.8:c.1742C>T
MANE Select
|
ENSP00000267845.3:p.Thr581Met
|
|
ENST00000267845.7:c.1742C>T
|
ENSP00000267845.3:p.Thr581Met
|
|
ENST00000543581.5:c.1643C>T
|
ENSP00000440252.1:p.Thr548Met
|
|
ENST00000559816.1:n.1486C>T
|
|
|
NM_001306146.1:c.1643C>T
|
NP_001293075.1:p.Thr548Met
|
|
NM_002112.3:c.1742C>T
|
NP_002103.2:p.Thr581Met
|
|
XM_011521479.1:c.1505C>T
|
XP_011519781.1:p.Thr502Met
|
|
XM_011521480.1:c.1310C>T
|
XP_011519782.1:p.Thr437Met
|
|
XM_017022094.1:c.1847C>T
|
XP_016877583.1:p.Thr616Met
|
|
XM_017022095.1:c.1748C>T
|
XP_016877584.1:p.Thr583Met
|
|
XM_017022096.1:c.1619C>T
|
XP_016877585.1:p.Thr540Met
|
|
XM_017022097.1:c.1610C>T
|
XP_016877586.1:p.Thr537Met
|
|
XM_017022098.1:c.1415C>T
|
XP_016877587.1:p.Thr472Met
|
|
NM_002112.4:c.1742C>T
MANE Select
|
NP_002103.2:p.Thr581Met
|
|
NM_001306146.2:c.1643C>T
|
NP_001293075.1:p.Thr548Met
|
|