ENST00000375559.8:c.1298T>C
MANE Select
|
ENSP00000364709.3:p.Val433Ala
|
|
ENST00000375551.7:c.*289T>C
|
ENSP00000364701.3:n.*289T>C
|
|
ENST00000375559.7:c.1298T>C
|
ENSP00000364709.3:p.Val433Ala
|
|
ENST00000409306.5:c.*289T>C
|
ENSP00000387092.1:n.*289T>C
|
|
NM_000504.3:c.1298T>C , LRG_548t1:c.1298T>C
|
NP_000495.1:p.Val433Ala
|
|
NM_001312674.1:c.1166T>C
|
NP_001299603.1:p.Val389Ala
|
|
NM_001312675.1:c.*289T>C
|
NP_001299604.1:n.*289T>C
|
|
NM_000504.4:c.1298T>C
MANE Select
|
NP_000495.1:p.Val433Ala
|
|
NM_001312674.2:c.1166T>C
|
NP_001299603.1:p.Val389Ala
|
|
NM_001312675.2:c.*289T>C
|
NP_001299604.1:n.*289T>C
|
|