ENST00000295897.9:c.1061T>A
MANE Select
|
ENSP00000295897.4:p.Phe354Tyr
|
|
ENST00000295897.8:c.1061T>A
|
ENSP00000295897.4:p.Phe354Tyr
|
|
ENST00000401494.7:c.716T>A
|
ENSP00000384695.3:p.Phe239Tyr
|
|
ENST00000415165.6:c.485T>A
|
ENSP00000401820.2:p.Phe162Tyr
|
|
ENST00000476441.6:c.*340T>A
|
ENSP00000423727.1:n.*340T>A
|
|
ENST00000484992.1:n.381T>A
|
|
|
ENST00000503124.5:c.611T>A
|
ENSP00000421027.1:p.Phe204Tyr
|
|
ENST00000504043.1:n.64T>A
|
|
|
ENST00000505649.5:n.747T>A
|
|
|
ENST00000509063.5:c.1061T>A
|
ENSP00000422784.1:p.Phe354Tyr
|
|
ENST00000511370.1:c.594T>A
|
|
|
ENST00000621085.4:c.491-69T>A
|
ENSP00000483421.1:n.491-69T>A
|
|
ENST00000621628.4:c.487-65T>A
|
ENSP00000480485.1:n.487-65T>A
|
|
NM_000477.5:c.1061T>A
|
NP_000468.1:p.Phe354Tyr
|
|
NM_000477.6:c.1061T>A
|
NP_000468.1:p.Phe354Tyr
|
|
NM_000477.7:c.1061T>A
MANE Select
|
NP_000468.1:p.Phe354Tyr
|
|