ENST00000553106.6:c.992T>A
MANE Select
|
ENSP00000448059.1:p.Phe331Tyr
|
|
ENST00000307000.7:c.977T>A
|
ENSP00000303500.2:p.Phe326Tyr
|
|
ENST00000549247.6:n.751T>A
|
|
|
ENST00000551114.2:n.654T>A
|
|
|
ENST00000553106.5:c.992T>A
|
ENSP00000448059.1:p.Phe331Tyr
|
|
ENST00000635477.1:c.96T>A
|
|
|
ENST00000635528.1:n.507T>A
|
|
|
NM_000277.1:c.992T>A
|
NP_000268.1:p.Phe331Tyr
|
|
XM_011538422.1:c.935T>A
|
XP_011536724.1:p.Phe312Tyr
|
|
NM_000277.2:c.992T>A
|
NP_000268.1:p.Phe331Tyr
|
|
NM_001354304.1:c.992T>A
|
NP_001341233.1:p.Phe331Tyr
|
|
NM_000277.3:c.992T>A
MANE Select
|
NP_000268.1:p.Phe331Tyr
|
|
NM_001354304.2:c.992T>A
|
NP_001341233.1:p.Phe331Tyr
|
|