ENST00000318158.11:c.557A>G
MANE Select
|
ENSP00000313432.6:p.Gln186Arg
|
|
ENST00000318158.10:c.557A>G
|
ENSP00000313432.6:p.Gln186Arg
|
|
ENST00000377824.8:n.594A>G
|
|
|
ENST00000460882.5:n.584A>G
|
|
|
ENST00000480596.5:n.1258A>G
|
|
|
ENST00000482603.1:n.10A>G
|
|
|
ENST00000491488.5:n.262A>G
|
|
|
ENST00000494290.1:c.128A>G
|
ENSP00000432021.1:p.Gln43Arg
|
|
ENST00000497693.1:n.2090A>G
|
|
|
ENST00000607784.1:c.557A>G
|
ENSP00000475569.1:p.Gln186Arg
|
|
NM_012203.1:c.557A>G
|
NP_036335.1:p.Gln186Arg
|
|
XM_005251631.1:c.236A>G
|
XP_005251688.1:p.Gln79Arg
|
|
XM_011518073.1:c.155A>G
|
XP_011516375.1:p.Gln52Arg
|
|
XR_929374.1:n.1002A>G
|
|
|
XM_017015320.2:c.557A>G
|
XP_016870809.1:p.Gln186Arg
|
|
XM_017015321.2:c.557A>G
|
XP_016870810.1:p.Gln186Arg
|
|
XM_017015323.2:c.155A>G
|
XP_016870812.1:p.Gln52Arg
|
|
XM_024447716.1:c.830A>G
|
XP_024303484.1:p.Gln277Arg
|
|
XM_024447717.1:c.830A>G
|
XP_024303485.1:p.Gln277Arg
|
|
XR_002956828.1:n.845A>G
|
|
|
XR_002956829.1:n.845A>G
|
|
|
XR_002956830.1:n.616A>G
|
|
|
XR_002956831.1:n.291A>G
|
|
|
XR_002956832.1:n.976A>G
|
|
|
NM_012203.2:c.557A>G
MANE Select
|
NP_036335.1:p.Gln186Arg
|
|