ENST00000398603.6:c.349G=
|
ENSP00000381604.1:p.Asp117=
|
|
ENST00000398606.10:c.457G=
MANE Select
|
ENSP00000381607.3:p.Asp153=
|
|
ENST00000646888.1:c.*173G=
|
ENSP00000494477.1:n.*173G=
|
|
ENST00000398603.5:c.349G=
|
ENSP00000381604.1:p.Asp117=
|
|
ENST00000398606.7:c.457G=
|
ENSP00000381607.3:p.Asp153=
|
|
ENST00000467591.1:n.568G=
|
|
|
ENST00000494593.1:n.1429G=
|
|
|
ENST00000495996.1:c.183G=
|
ENSP00000484686.1:p.Leu61=
|
|
ENST00000498765.5:c.520G=
|
|
|
NM_000852.3:c.457G= , LRG_723t1:c.457G=
|
NP_000843.1:p.Asp153=
|
|
NM_000852.4:c.457G=
MANE Select
|
NP_000843.1:p.Asp153=
|
|