ENST00000295897.9:c.*2A>C
MANE Select
|
ENSP00000295897.4:n.*2A>C
|
|
ENST00000295897.8:c.*2A>C
|
ENSP00000295897.4:n.*2A>C
|
|
ENST00000401494.7:c.*2A>C
|
ENSP00000384695.3:n.*2A>C
|
|
ENST00000415165.6:c.*2A>C
|
ENSP00000401820.2:n.*2A>C
|
|
ENST00000476441.6:c.*1111A>C
|
ENSP00000423727.1:n.*1111A>C
|
|
ENST00000495173.1:n.140A>C
|
|
|
ENST00000503124.5:c.*2A>C
|
ENSP00000421027.1:n.*2A>C
|
|
ENST00000505649.5:n.1379A>C
|
|
|
ENST00000508932.5:n.222A>C
|
|
|
ENST00000509063.5:c.1785+661A>C
|
ENSP00000422784.1:n.1785+661A>C
|
|
ENST00000511370.1:c.1365A>C
|
|
|
ENST00000621085.4:c.*2A>C
|
ENSP00000483421.1:n.*2A>C
|
|
ENST00000621628.4:c.*2A>C
|
ENSP00000480485.1:n.*2A>C
|
|
NM_000477.5:c.*2A>C
|
NP_000468.1:n.*2A>C
|
|
NM_000477.6:c.*2A>C
|
NP_000468.1:n.*2A>C
|
|
NM_000477.7:c.*2A>C
MANE Select
|
NP_000468.1:n.*2A>C
|
|