ENST00000398603.6:c.351C>A
|
ENSP00000381604.1:p.Asp117Glu
|
|
ENST00000398606.10:c.459C>A
MANE Select
|
ENSP00000381607.3:p.Asp153Glu
|
|
ENST00000646888.1:c.*175C>A
|
ENSP00000494477.1:n.*175C>A
|
|
ENST00000398603.5:c.351C>A
|
ENSP00000381604.1:p.Asp117Glu
|
|
ENST00000398606.7:c.459C>A
|
ENSP00000381607.3:p.Asp153Glu
|
|
ENST00000467591.1:n.570C>A
|
|
|
ENST00000494593.1:n.1431C>A
|
|
|
ENST00000495996.1:c.185C>A
|
ENSP00000484686.1:p.Thr62Asn
|
|
ENST00000498765.5:c.522C>A
|
|
|
NM_000852.3:c.459C>A , LRG_723t1:c.459C>A
|
NP_000843.1:p.Asp153Glu
|
|
NM_000852.4:c.459C>A
MANE Select
|
NP_000843.1:p.Asp153Glu
|
|