ENST00000375559.8:c.1193T>C
MANE Select
|
ENSP00000364709.3:p.Ile398Thr
|
|
ENST00000375551.7:c.*184T>C
|
ENSP00000364701.3:n.*184T>C
|
|
ENST00000375559.7:c.1193T>C
|
ENSP00000364709.3:p.Ile398Thr
|
|
ENST00000409306.5:c.*184T>C
|
ENSP00000387092.1:n.*184T>C
|
|
NM_000504.3:c.1193T>C , LRG_548t1:c.1193T>C
|
NP_000495.1:p.Ile398Thr
|
|
NM_001312674.1:c.1061T>C
|
NP_001299603.1:p.Ile354Thr
|
|
NM_001312675.1:c.*184T>C
|
NP_001299604.1:n.*184T>C
|
|
NM_000504.4:c.1193T>C
MANE Select
|
NP_000495.1:p.Ile398Thr
|
|
NM_001312674.2:c.1061T>C
|
NP_001299603.1:p.Ile354Thr
|
|
NM_001312675.2:c.*184T>C
|
NP_001299604.1:n.*184T>C
|
|