ENST00000696170.1:c.*38A>T
|
ENSP00000512461.1:n.*38A>T
|
|
ENST00000696171.1:c.433A>T
|
ENSP00000512462.1:p.Ile145Phe
|
|
ENST00000696172.1:c.338-2959A>T
|
ENSP00000512463.1:n.338-2959A>T
|
|
ENST00000378588.5:c.529A>T
MANE Select
|
ENSP00000367851.4:p.Ile177Phe
|
|
ENST00000378588.4:c.529A>T
|
ENSP00000367851.4:p.Ile177Phe
|
|
ENST00000465127.1:c.171+369996A>T
|
ENSP00000417050.1:n.171+369996A>T
|
|
NM_000397.3:c.529A>T , LRG_53t1:c.529A>T
|
NP_000388.2:p.Ile177Phe
|
|
XM_011543890.1:c.223A>T
|
XP_011542192.1:p.Ile75Phe
|
|
NM_000397.4:c.529A>T
MANE Select
|
NP_000388.2:p.Ile177Phe
|
|