ENST00000342741.6:c.773A>G
MANE Select
|
ENSP00000339933.4:p.Gln258Arg
|
|
ENST00000342741.4:c.773A>G
|
ENSP00000339933.4:p.Gln258Arg
|
|
ENST00000392414.7:c.680A>G
|
ENSP00000376214.3:p.Gln227Arg
|
|
NM_000298.5:c.773A>G
|
NP_000289.1:p.Gln258Arg
|
|
NM_181871.3:c.680A>G
|
NP_870986.1:p.Gln227Arg
|
|
XM_005245266.3:c.932A>G
|
XP_005245323.1:p.Gln311Arg
|
|
XM_006711386.2:c.581A>G
|
XP_006711449.1:p.Gln194Arg
|
|
XM_011509639.1:c.932A>G
|
XP_011507941.1:p.Gln311Arg
|
|
XM_011509640.1:c.581A>G
|
XP_011507942.1:p.Gln194Arg
|
|
NM_000298.6:c.773A>G
MANE Select
|
NP_000289.1:p.Gln258Arg
|
|
XM_006711386.4:c.581A>G
|
XP_006711449.1:p.Gln194Arg
|
|
XM_011509640.3:c.581A>G
|
XP_011507942.1:p.Gln194Arg
|
|
XM_017001493.1:c.773A>G
|
XP_016856982.1:p.Gln258Arg
|
|
NM_181871.4:c.680A>G
|
NP_870986.1:p.Gln227Arg
|
|