ENST00000328300.11:c.4782G>T
MANE Select
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ENSP00000331902.7:p.Gln1594His
|
|
ENST00000361603.7:c.4764G>T
|
ENSP00000354505.2:p.Gln1588His
|
|
ENST00000510690.2:n.1276G>T
|
|
|
ENST00000644079.1:n.1268G>T
|
|
|
ENST00000328300.10:c.4782G>T
|
ENSP00000331902.6:p.Gln1594His
|
|
ENST00000361603.6:c.4764G>T
|
ENSP00000354505.2:p.Gln1588His
|
|
ENST00000504541.1:c.180G>T
|
ENSP00000424845.1:p.Gln60His
|
|
ENST00000515658.1:c.325-1415G>T
|
|
|
NM_000495.4:c.4764G>T
|
NP_000486.1:p.Gln1588His
|
|
NM_033380.2:c.4782G>T
|
NP_203699.1:p.Gln1594His
|
|
XM_005262070.2:c.4773G>T
|
XP_005262127.1:p.Gln1591His
|
|
XM_006724616.2:c.4782G>T
|
XP_006724679.1:p.Gln1594His
|
|
XM_011530849.1:c.4458G>T
|
XP_011529151.1:p.Gln1486His
|
|
XM_011530851.1:c.2355G>T
|
XP_011529153.1:p.Gln785His
|
|
XM_011530849.2:c.4797G>T
|
XP_011529151.2:p.Gln1599His
|
|
XM_017029259.2:c.4788G>T
|
XP_016884748.1:p.Gln1596His
|
|
XM_017029260.1:c.4779G>T
|
XP_016884749.1:p.Gln1593His
|
|
XM_017029263.2:c.3117G>T
|
XP_016884752.1:p.Gln1039His
|
|
NM_000495.5:c.4764G>T
|
NP_000486.1:p.Gln1588His
|
|
NM_033380.3:c.4782G>T
MANE Select
|
NP_203699.1:p.Gln1594His
|
|