ENST00000267845.8:c.1785G>T
MANE Select
|
ENSP00000267845.3:p.Gln595His
|
|
ENST00000267845.7:c.1785G>T
|
ENSP00000267845.3:p.Gln595His
|
|
ENST00000543581.5:c.1686G>T
|
ENSP00000440252.1:p.Gln562His
|
|
ENST00000559816.1:n.1529G>T
|
|
|
NM_001306146.1:c.1686G>T
|
NP_001293075.1:p.Gln562His
|
|
NM_002112.3:c.1785G>T
|
NP_002103.2:p.Gln595His
|
|
XM_011521479.1:c.1548G>T
|
XP_011519781.1:p.Gln516His
|
|
XM_011521480.1:c.1353G>T
|
XP_011519782.1:p.Gln451His
|
|
XM_017022094.1:c.1890G>T
|
XP_016877583.1:p.Gln630His
|
|
XM_017022095.1:c.1791G>T
|
XP_016877584.1:p.Gln597His
|
|
XM_017022096.1:c.1662G>T
|
XP_016877585.1:p.Gln554His
|
|
XM_017022097.1:c.1653G>T
|
XP_016877586.1:p.Gln551His
|
|
XM_017022098.1:c.1458G>T
|
XP_016877587.1:p.Gln486His
|
|
NM_002112.4:c.1785G>T
MANE Select
|
NP_002103.2:p.Gln595His
|
|
NM_001306146.2:c.1686G>T
|
NP_001293075.1:p.Gln562His
|
|