ENST00000328300.11:c.3881G>T
MANE Select
|
ENSP00000331902.7:p.Gly1294Val
|
|
ENST00000361603.7:c.3863G>T
|
ENSP00000354505.2:p.Gly1288Val
|
|
ENST00000510690.2:n.375G>T
|
|
|
ENST00000328300.10:c.3881G>T
|
ENSP00000331902.6:p.Gly1294Val
|
|
ENST00000361603.6:c.3863G>T
|
ENSP00000354505.2:p.Gly1288Val
|
|
ENST00000489230.1:n.284G>T
|
|
|
ENST00000510690.1:n.375G>T
|
|
|
NM_000495.4:c.3863G>T
|
NP_000486.1:p.Gly1288Val
|
|
NM_033380.2:c.3881G>T
|
NP_203699.1:p.Gly1294Val
|
|
XM_005262070.2:c.3872G>T
|
XP_005262127.1:p.Gly1291Val
|
|
XM_006724616.2:c.3881G>T
|
XP_006724679.1:p.Gly1294Val
|
|
XM_011530849.1:c.3557G>T
|
XP_011529151.1:p.Gly1186Val
|
|
XM_011530851.1:c.1454G>T
|
XP_011529153.1:p.Gly485Val
|
|
XM_011530849.2:c.3896G>T
|
XP_011529151.2:p.Gly1299Val
|
|
XM_017029259.2:c.3887G>T
|
XP_016884748.1:p.Gly1296Val
|
|
XM_017029260.1:c.3878G>T
|
XP_016884749.1:p.Gly1293Val
|
|
XM_017029261.1:c.3896G>T
|
XP_016884750.1:p.Gly1299Val
|
|
XM_017029263.2:c.2216G>T
|
XP_016884752.1:p.Gly739Val
|
|
NM_000495.5:c.3863G>T
|
NP_000486.1:p.Gly1288Val
|
|
NM_033380.3:c.3881G>T
MANE Select
|
NP_203699.1:p.Gly1294Val
|
|