ENST00000398603.6:c.336+397_336+398delinsGA
|
ENSP00000381604.1:n.336+397_336+398delinsGA
|
|
ENST00000398606.10:c.336+397_336+398delinsGA
MANE Select
|
ENSP00000381607.3:n.336+397_336+398delinsGA
|
|
ENST00000646888.1:c.*52+397_*52+398delinsGA
|
ENSP00000494477.1:n.*52+397_*52+398delinsGA
|
|
ENST00000398603.5:c.336+397_336+398delinsGA
|
ENSP00000381604.1:n.336+397_336+398delinsGA
|
|
ENST00000398606.7:c.336+397_336+398delinsGA
|
ENSP00000381607.3:n.336+397_336+398delinsGA
|
|
ENST00000467591.1:n.447+397_447+398delinsGA
|
|
|
ENST00000494593.1:n.1131+397_1131+398delinsGA
|
|
|
ENST00000498765.5:c.399+397_399+398delinsGA
|
|
|
NM_000852.3:c.336+397_336+398delinsGA , LRG_723t1:c.336+397_336+398delinsGA
|
NP_000843.1:n.336+397_336+398delinsGA
|
|
NM_000852.4:c.336+397_336+398delinsGA
MANE Select
|
NP_000843.1:n.336+397_336+398delinsGA
|
|