ENST00000696133.1:c.1297G>T
|
ENSP00000512426.1:p.Val433Phe
|
|
ENST00000696134.1:c.*724G>T
|
ENSP00000512427.1:n.*724G>T
|
|
ENST00000367021.8:c.1297G>T
MANE Select
|
ENSP00000355988.3:p.Val433Phe
|
|
ENST00000643798.1:c.*807G>T
|
ENSP00000496669.1:n.*807G>T
|
|
ENST00000367021.7:c.1297G>T
|
ENSP00000355988.3:p.Val433Phe
|
|
ENST00000542854.5:c.1012G>T
|
ENSP00000440532.1:p.Val338Phe
|
|
NM_001206696.1:c.1012G>T
|
NP_001193625.1:p.Val338Phe
|
|
NM_006147.3:c.1297G>T
|
NP_006138.1:p.Val433Phe
|
|
NM_006147.4:c.1297G>T
MANE Select
|
NP_006138.1:p.Val433Phe
|
|
NM_001206696.2:c.1012G>T
|
NP_001193625.1:p.Val338Phe
|
|