ENST00000328300.11:c.4813T>G
MANE Select
|
ENSP00000331902.7:p.Phe1605Val
|
|
ENST00000361603.7:c.4795T>G
|
ENSP00000354505.2:p.Phe1599Val
|
|
ENST00000510690.2:n.1307T>G
|
|
|
ENST00000644079.1:n.1299T>G
|
|
|
ENST00000328300.10:c.4813T>G
|
ENSP00000331902.6:p.Phe1605Val
|
|
ENST00000361603.6:c.4795T>G
|
ENSP00000354505.2:p.Phe1599Val
|
|
ENST00000504541.1:c.211T>G
|
ENSP00000424845.1:p.Phe71Val
|
|
ENST00000515658.1:c.325-1384T>G
|
|
|
NM_000495.4:c.4795T>G
|
NP_000486.1:p.Phe1599Val
|
|
NM_033380.2:c.4813T>G
|
NP_203699.1:p.Phe1605Val
|
|
XM_005262070.2:c.4804T>G
|
XP_005262127.1:p.Phe1602Val
|
|
XM_006724616.2:c.4813T>G
|
XP_006724679.1:p.Phe1605Val
|
|
XM_011530849.1:c.4489T>G
|
XP_011529151.1:p.Phe1497Val
|
|
XM_011530851.1:c.2386T>G
|
XP_011529153.1:p.Phe796Val
|
|
XM_011530849.2:c.4828T>G
|
XP_011529151.2:p.Phe1610Val
|
|
XM_017029259.2:c.4819T>G
|
XP_016884748.1:p.Phe1607Val
|
|
XM_017029260.1:c.4810T>G
|
XP_016884749.1:p.Phe1604Val
|
|
XM_017029263.2:c.3148T>G
|
XP_016884752.1:p.Phe1050Val
|
|
NM_000495.5:c.4795T>G
|
NP_000486.1:p.Phe1599Val
|
|
NM_033380.3:c.4813T>G
MANE Select
|
NP_203699.1:p.Phe1605Val
|
|