ENST00000267845.8:c.1944A>C
MANE Select
|
ENSP00000267845.3:p.Gln648His
|
|
ENST00000267845.7:c.1944A>C
|
ENSP00000267845.3:p.Gln648His
|
|
ENST00000543581.5:c.1845A>C
|
ENSP00000440252.1:p.Gln615His
|
|
ENST00000559816.1:n.1688A>C
|
|
|
NM_001306146.1:c.1845A>C
|
NP_001293075.1:p.Gln615His
|
|
NM_002112.3:c.1944A>C
|
NP_002103.2:p.Gln648His
|
|
XM_011521479.1:c.1707A>C
|
XP_011519781.1:p.Gln569His
|
|
XM_011521480.1:c.1512A>C
|
XP_011519782.1:p.Gln504His
|
|
XM_017022094.1:c.2049A>C
|
XP_016877583.1:p.Gln683His
|
|
XM_017022095.1:c.1950A>C
|
XP_016877584.1:p.Gln650His
|
|
XM_017022096.1:c.1821A>C
|
XP_016877585.1:p.Gln607His
|
|
XM_017022097.1:c.1812A>C
|
XP_016877586.1:p.Gln604His
|
|
XM_017022098.1:c.1617A>C
|
XP_016877587.1:p.Gln539His
|
|
NM_002112.4:c.1944A>C
MANE Select
|
NP_002103.2:p.Gln648His
|
|
NM_001306146.2:c.1845A>C
|
NP_001293075.1:p.Gln615His
|
|