ENST00000267845.8:c.1714T>C
MANE Select
|
ENSP00000267845.3:p.Tyr572His
|
|
ENST00000267845.7:c.1714T>C
|
ENSP00000267845.3:p.Tyr572His
|
|
ENST00000543581.5:c.1615T>C
|
ENSP00000440252.1:p.Tyr539His
|
|
ENST00000559816.1:n.1458T>C
|
|
|
NM_001306146.1:c.1615T>C
|
NP_001293075.1:p.Tyr539His
|
|
NM_002112.3:c.1714T>C
|
NP_002103.2:p.Tyr572His
|
|
XM_011521479.1:c.1477T>C
|
XP_011519781.1:p.Tyr493His
|
|
XM_011521480.1:c.1282T>C
|
XP_011519782.1:p.Tyr428His
|
|
XM_017022094.1:c.1819T>C
|
XP_016877583.1:p.Tyr607His
|
|
XM_017022095.1:c.1720T>C
|
XP_016877584.1:p.Tyr574His
|
|
XM_017022096.1:c.1591T>C
|
XP_016877585.1:p.Tyr531His
|
|
XM_017022097.1:c.1582T>C
|
XP_016877586.1:p.Tyr528His
|
|
XM_017022098.1:c.1387T>C
|
XP_016877587.1:p.Tyr463His
|
|
NM_002112.4:c.1714T>C
MANE Select
|
NP_002103.2:p.Tyr572His
|
|
NM_001306146.2:c.1615T>C
|
NP_001293075.1:p.Tyr539His
|
|