ENST00000328300.11:c.3942G>C
MANE Select
|
ENSP00000331902.7:p.Gln1314His
|
|
ENST00000361603.7:c.3924G>C
|
ENSP00000354505.2:p.Gln1308His
|
|
ENST00000510690.2:n.436G>C
|
|
|
ENST00000328300.10:c.3942G>C
|
ENSP00000331902.6:p.Gln1314His
|
|
ENST00000361603.6:c.3924G>C
|
ENSP00000354505.2:p.Gln1308His
|
|
ENST00000489230.1:n.345G>C
|
|
|
NM_000495.4:c.3924G>C
|
NP_000486.1:p.Gln1308His
|
|
NM_033380.2:c.3942G>C
|
NP_203699.1:p.Gln1314His
|
|
XM_005262070.2:c.3933G>C
|
XP_005262127.1:p.Gln1311His
|
|
XM_006724616.2:c.3942G>C
|
XP_006724679.1:p.Gln1314His
|
|
XM_011530849.1:c.3618G>C
|
XP_011529151.1:p.Gln1206His
|
|
XM_011530851.1:c.1515G>C
|
XP_011529153.1:p.Gln505His
|
|
XM_011530849.2:c.3957G>C
|
XP_011529151.2:p.Gln1319His
|
|
XM_017029259.2:c.3948G>C
|
XP_016884748.1:p.Gln1316His
|
|
XM_017029260.1:c.3939G>C
|
XP_016884749.1:p.Gln1313His
|
|
XM_017029261.1:c.3957G>C
|
XP_016884750.1:p.Gln1319His
|
|
XM_017029263.2:c.2277G>C
|
XP_016884752.1:p.Gln759His
|
|
NM_000495.5:c.3924G>C
|
NP_000486.1:p.Gln1308His
|
|
NM_033380.3:c.3942G>C
MANE Select
|
NP_203699.1:p.Gln1314His
|
|