ENST00000398603.6:c.381T=
|
ENSP00000381604.1:p.His127=
|
|
ENST00000398606.10:c.489T=
MANE Select
|
ENSP00000381607.3:p.His163=
|
|
ENST00000646888.1:c.*205T=
|
ENSP00000494477.1:n.*205T=
|
|
ENST00000398603.5:c.381T=
|
ENSP00000381604.1:p.His127=
|
|
ENST00000398606.7:c.489T=
|
ENSP00000381607.3:p.His163=
|
|
ENST00000467591.1:n.600T=
|
|
|
ENST00000494593.1:n.1461T=
|
|
|
ENST00000495996.1:c.215T=
|
ENSP00000484686.1:n.215T=
|
|
ENST00000498765.5:c.552T=
|
|
|
NM_000852.3:c.489T= , LRG_723t1:c.489T=
|
NP_000843.1:p.His163=
|
|
NM_000852.4:c.489T=
MANE Select
|
NP_000843.1:p.His163=
|
|