ENST00000267845.8:c.1976A>G
MANE Select
|
ENSP00000267845.3:p.Gln659Arg
|
|
ENST00000267845.7:c.1976A>G
|
ENSP00000267845.3:p.Gln659Arg
|
|
ENST00000543581.5:c.1877A>G
|
ENSP00000440252.1:p.Gln626Arg
|
|
ENST00000559816.1:n.1720A>G
|
|
|
NM_001306146.1:c.1877A>G
|
NP_001293075.1:p.Gln626Arg
|
|
NM_002112.3:c.1976A>G
|
NP_002103.2:p.Gln659Arg
|
|
XM_011521479.1:c.1739A>G
|
XP_011519781.1:p.Gln580Arg
|
|
XM_011521480.1:c.1544A>G
|
XP_011519782.1:p.Gln515Arg
|
|
XM_017022094.1:c.2081A>G
|
XP_016877583.1:p.Gln694Arg
|
|
XM_017022095.1:c.1982A>G
|
XP_016877584.1:p.Gln661Arg
|
|
XM_017022096.1:c.1853A>G
|
XP_016877585.1:p.Gln618Arg
|
|
XM_017022097.1:c.1844A>G
|
XP_016877586.1:p.Gln615Arg
|
|
XM_017022098.1:c.1649A>G
|
XP_016877587.1:p.Gln550Arg
|
|
NM_002112.4:c.1976A>G
MANE Select
|
NP_002103.2:p.Gln659Arg
|
|
NM_001306146.2:c.1877A>G
|
NP_001293075.1:p.Gln626Arg
|
|