ENST00000295897.9:c.*17A>G
MANE Select
|
ENSP00000295897.4:n.*17A>G
|
|
ENST00000295897.8:c.*17A>G
|
ENSP00000295897.4:n.*17A>G
|
|
ENST00000401494.7:c.*17A>G
|
ENSP00000384695.3:n.*17A>G
|
|
ENST00000415165.6:c.*17A>G
|
ENSP00000401820.2:n.*17A>G
|
|
ENST00000476441.6:c.*1126A>G
|
ENSP00000423727.1:n.*1126A>G
|
|
ENST00000495173.1:n.155A>G
|
|
|
ENST00000503124.5:c.*17A>G
|
ENSP00000421027.1:n.*17A>G
|
|
ENST00000505649.5:n.1394A>G
|
|
|
ENST00000508932.5:n.237A>G
|
|
|
ENST00000509063.5:c.1785+676A>G
|
ENSP00000422784.1:n.1785+676A>G
|
|
ENST00000511370.1:c.1380A>G
|
|
|
ENST00000621085.4:c.*17A>G
|
ENSP00000483421.1:n.*17A>G
|
|
ENST00000621628.4:c.*17A>G
|
ENSP00000480485.1:n.*17A>G
|
|
NM_000477.5:c.*17A>G
|
NP_000468.1:n.*17A>G
|
|
NM_000477.6:c.*17A>G
|
NP_000468.1:n.*17A>G
|
|
NM_000477.7:c.*17A>G
MANE Select
|
NP_000468.1:n.*17A>G
|
|