ENST00000328300.11:c.4264T>G
MANE Select
|
ENSP00000331902.7:p.Phe1422Val
|
|
ENST00000361603.7:c.4246T>G
|
ENSP00000354505.2:p.Phe1416Val
|
|
ENST00000510690.2:n.758T>G
|
|
|
ENST00000328300.10:c.4264T>G
|
ENSP00000331902.6:p.Phe1422Val
|
|
ENST00000361603.6:c.4246T>G
|
ENSP00000354505.2:p.Phe1416Val
|
|
ENST00000489230.1:n.667T>G
|
|
|
ENST00000515658.1:c.60T>G
|
|
|
NM_000495.4:c.4246T>G
|
NP_000486.1:p.Phe1416Val
|
|
NM_033380.2:c.4264T>G
|
NP_203699.1:p.Phe1422Val
|
|
XM_005262070.2:c.4255T>G
|
XP_005262127.1:p.Phe1419Val
|
|
XM_006724616.2:c.4264T>G
|
XP_006724679.1:p.Phe1422Val
|
|
XM_011530849.1:c.3940T>G
|
XP_011529151.1:p.Phe1314Val
|
|
XM_011530851.1:c.1837T>G
|
XP_011529153.1:p.Phe613Val
|
|
XM_011530849.2:c.4279T>G
|
XP_011529151.2:p.Phe1427Val
|
|
XM_017029259.2:c.4270T>G
|
XP_016884748.1:p.Phe1424Val
|
|
XM_017029260.1:c.4261T>G
|
XP_016884749.1:p.Phe1421Val
|
|
XM_017029263.2:c.2599T>G
|
XP_016884752.1:p.Phe867Val
|
|
NM_000495.5:c.4246T>G
|
NP_000486.1:p.Phe1416Val
|
|
NM_033380.3:c.4264T>G
MANE Select
|
NP_203699.1:p.Phe1422Val
|
|