ENST00000328300.11:c.3885A>T
MANE Select
|
ENSP00000331902.7:p.Gln1295His
|
|
ENST00000361603.7:c.3867A>T
|
ENSP00000354505.2:p.Gln1289His
|
|
ENST00000510690.2:n.379A>T
|
|
|
ENST00000328300.10:c.3885A>T
|
ENSP00000331902.6:p.Gln1295His
|
|
ENST00000361603.6:c.3867A>T
|
ENSP00000354505.2:p.Gln1289His
|
|
ENST00000489230.1:n.288A>T
|
|
|
ENST00000510690.1:n.379A>T
|
|
|
NM_000495.4:c.3867A>T
|
NP_000486.1:p.Gln1289His
|
|
NM_033380.2:c.3885A>T
|
NP_203699.1:p.Gln1295His
|
|
XM_005262070.2:c.3876A>T
|
XP_005262127.1:p.Gln1292His
|
|
XM_006724616.2:c.3885A>T
|
XP_006724679.1:p.Gln1295His
|
|
XM_011530849.1:c.3561A>T
|
XP_011529151.1:p.Gln1187His
|
|
XM_011530851.1:c.1458A>T
|
XP_011529153.1:p.Gln486His
|
|
XM_011530849.2:c.3900A>T
|
XP_011529151.2:p.Gln1300His
|
|
XM_017029259.2:c.3891A>T
|
XP_016884748.1:p.Gln1297His
|
|
XM_017029260.1:c.3882A>T
|
XP_016884749.1:p.Gln1294His
|
|
XM_017029261.1:c.3900A>T
|
XP_016884750.1:p.Gln1300His
|
|
XM_017029263.2:c.2220A>T
|
XP_016884752.1:p.Gln740His
|
|
NM_000495.5:c.3867A>T
|
NP_000486.1:p.Gln1289His
|
|
NM_033380.3:c.3885A>T
MANE Select
|
NP_203699.1:p.Gln1295His
|
|