ENST00000295897.9:c.1059-401T>C
MANE Select
|
ENSP00000295897.4:n.1059-401T>C
|
|
ENST00000295897.8:c.1059-401T>C
|
ENSP00000295897.4:n.1059-401T>C
|
|
ENST00000401494.7:c.714-401T>C
|
ENSP00000384695.3:n.714-401T>C
|
|
ENST00000415165.6:c.483-401T>C
|
ENSP00000401820.2:n.483-401T>C
|
|
ENST00000476441.6:c.*338-401T>C
|
ENSP00000423727.1:n.*338-401T>C
|
|
ENST00000484992.1:n.379-401T>C
|
|
|
ENST00000503124.5:c.609-401T>C
|
ENSP00000421027.1:n.609-401T>C
|
|
ENST00000504043.1:n.62-401T>C
|
|
|
ENST00000505649.5:n.745-401T>C
|
|
|
ENST00000509063.5:c.1059-401T>C
|
ENSP00000422784.1:n.1059-401T>C
|
|
ENST00000511370.1:c.592-401T>C
|
|
|
ENST00000621085.4:c.491-472T>C
|
ENSP00000483421.1:n.491-472T>C
|
|
ENST00000621628.4:c.487-468T>C
|
ENSP00000480485.1:n.487-468T>C
|
|
NM_000477.5:c.1059-401T>C
|
NP_000468.1:n.1059-401T>C
|
|
NM_000477.6:c.1059-401T>C
|
NP_000468.1:n.1059-401T>C
|
|
NM_000477.7:c.1059-401T>C
MANE Select
|
NP_000468.1:n.1059-401T>C
|
|