ENST00000328300.11:c.4443A>C
MANE Select
|
ENSP00000331902.7:p.Gln1481His
|
|
ENST00000361603.7:c.4425A>C
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ENSP00000354505.2:p.Gln1475His
|
|
ENST00000510690.2:n.937A>C
|
|
|
ENST00000328300.10:c.4443A>C
|
ENSP00000331902.6:p.Gln1481His
|
|
ENST00000361603.6:c.4425A>C
|
ENSP00000354505.2:p.Gln1475His
|
|
ENST00000515658.1:c.239A>C
|
|
|
NM_000495.4:c.4425A>C
|
NP_000486.1:p.Gln1475His
|
|
NM_033380.2:c.4443A>C
|
NP_203699.1:p.Gln1481His
|
|
XM_005262070.2:c.4434A>C
|
XP_005262127.1:p.Gln1478His
|
|
XM_006724616.2:c.4443A>C
|
XP_006724679.1:p.Gln1481His
|
|
XM_011530849.1:c.4119A>C
|
XP_011529151.1:p.Gln1373His
|
|
XM_011530851.1:c.2016A>C
|
XP_011529153.1:p.Gln672His
|
|
XM_011530849.2:c.4458A>C
|
XP_011529151.2:p.Gln1486His
|
|
XM_017029259.2:c.4449A>C
|
XP_016884748.1:p.Gln1483His
|
|
XM_017029260.1:c.4440A>C
|
XP_016884749.1:p.Gln1480His
|
|
XM_017029263.2:c.2778A>C
|
XP_016884752.1:p.Gln926His
|
|
NM_000495.5:c.4425A>C
|
NP_000486.1:p.Gln1475His
|
|
NM_033380.3:c.4443A>C
MANE Select
|
NP_203699.1:p.Gln1481His
|
|