ENST00000398603.6:c.406_407delinsGA
|
ENSP00000381604.1:p.Asp136=
|
|
ENST00000398606.10:c.514_515delinsGA
MANE Select
|
ENSP00000381607.3:p.Asp172=
|
|
ENST00000646888.1:c.*230_*231delinsGA
|
ENSP00000494477.1:n.*230_*231delinsGA
|
|
ENST00000398603.5:c.406_407delinsGA
|
ENSP00000381604.1:p.Asp136=
|
|
ENST00000398606.7:c.514_515delinsGA
|
ENSP00000381607.3:p.Asp172=
|
|
ENST00000467591.1:n.625_626delinsGA
|
|
|
ENST00000494593.1:n.1486_1487delinsGA
|
|
|
ENST00000498765.5:c.577_578delinsGA
|
|
|
NM_000852.3:c.514_515delinsGA , LRG_723t1:c.514_515delinsGA
|
NP_000843.1:p.Asp172=
|
|
NM_000852.4:c.514_515delinsGA
MANE Select
|
NP_000843.1:p.Asp172=
|
|