ENST00000295897.9:c.1592T>A
MANE Select
|
ENSP00000295897.4:p.Phe531Tyr
|
|
ENST00000295897.8:c.1592T>A
|
ENSP00000295897.4:p.Phe531Tyr
|
|
ENST00000401494.7:c.1247T>A
|
ENSP00000384695.3:p.Phe416Tyr
|
|
ENST00000415165.6:c.1016T>A
|
ENSP00000401820.2:p.Phe339Tyr
|
|
ENST00000476441.6:c.*871T>A
|
ENSP00000423727.1:n.*871T>A
|
|
ENST00000486939.1:n.246T>A
|
|
|
ENST00000503124.5:c.1142T>A
|
ENSP00000421027.1:p.Phe381Tyr
|
|
ENST00000505649.5:n.1139T>A
|
|
|
ENST00000509063.5:c.1592T>A
|
ENSP00000422784.1:p.Phe531Tyr
|
|
ENST00000511370.1:c.1125T>A
|
|
|
ENST00000621085.4:c.953T>A
|
ENSP00000483421.1:p.Phe318Tyr
|
|
ENST00000621628.4:c.953T>A
|
ENSP00000480485.1:p.Phe318Tyr
|
|
NM_000477.5:c.1592T>A
|
NP_000468.1:p.Phe531Tyr
|
|
NM_000477.6:c.1592T>A
|
NP_000468.1:p.Phe531Tyr
|
|
NM_000477.7:c.1592T>A
MANE Select
|
NP_000468.1:p.Phe531Tyr
|
|