ENST00000682028.1:c.529G>T
|
ENSP00000507230.1:p.Val177Phe
|
|
ENST00000682268.1:n.827G>T
|
|
|
ENST00000682902.1:n.831G>T
|
|
|
ENST00000683513.1:c.529G>T
|
ENSP00000506809.1:p.Val177Phe
|
|
ENST00000263431.4:c.529G>T
MANE Select
|
ENSP00000263431.3:p.Val177Phe
|
|
ENST00000263431.3:c.529G>T
|
ENSP00000263431.3:p.Val177Phe
|
|
ENST00000474397.5:c.145G>T
|
ENSP00000471271.1:p.Val49Phe
|
|
NM_001316329.1:c.529G>T
|
NP_001303258.1:p.Val177Phe
|
|
NM_002739.3:c.529G>T , LRG_669t1:c.529G>T
|
NP_002730.1:p.Val177Phe
|
|
NM_002739.4:c.529G>T
|
NP_002730.1:p.Val177Phe
|
|
NM_002739.5:c.529G>T
MANE Select
|
NP_002730.1:p.Val177Phe
|
|
NM_001316329.2:c.529G>T
|
NP_001303258.1:p.Val177Phe
|
|