ENST00000295897.9:c.1094A>T
MANE Select
|
ENSP00000295897.4:p.Tyr365Phe
|
|
ENST00000295897.8:c.1094A>T
|
ENSP00000295897.4:p.Tyr365Phe
|
|
ENST00000401494.7:c.749A>T
|
ENSP00000384695.3:p.Tyr250Phe
|
|
ENST00000415165.6:c.518A>T
|
ENSP00000401820.2:p.Tyr173Phe
|
|
ENST00000476441.6:c.*373A>T
|
ENSP00000423727.1:n.*373A>T
|
|
ENST00000484992.1:n.414A>T
|
|
|
ENST00000503124.5:c.644A>T
|
ENSP00000421027.1:p.Tyr215Phe
|
|
ENST00000504043.1:n.97A>T
|
|
|
ENST00000505649.5:n.780A>T
|
|
|
ENST00000509063.5:c.1094A>T
|
ENSP00000422784.1:p.Tyr365Phe
|
|
ENST00000511370.1:c.627A>T
|
|
|
ENST00000621085.4:c.491-36A>T
|
ENSP00000483421.1:n.491-36A>T
|
|
ENST00000621628.4:c.487-32A>T
|
ENSP00000480485.1:n.487-32A>T
|
|
NM_000477.5:c.1094A>T
|
NP_000468.1:p.Tyr365Phe
|
|
NM_000477.6:c.1094A>T
|
NP_000468.1:p.Tyr365Phe
|
|
NM_000477.7:c.1094A>T
MANE Select
|
NP_000468.1:p.Tyr365Phe
|
|