ENST00000696170.1:c.*75T>A
|
ENSP00000512461.1:n.*75T>A
|
|
ENST00000696171.1:c.470T>A
|
ENSP00000512462.1:p.Ile157Asn
|
|
ENST00000696172.1:c.338-2922T>A
|
ENSP00000512463.1:n.338-2922T>A
|
|
ENST00000378588.5:c.566T>A
MANE Select
|
ENSP00000367851.4:p.Ile189Asn
|
|
ENST00000378588.4:c.566T>A
|
ENSP00000367851.4:p.Ile189Asn
|
|
ENST00000465127.1:c.171+370033T>A
|
ENSP00000417050.1:n.171+370033T>A
|
|
NM_000397.3:c.566T>A , LRG_53t1:c.566T>A
|
NP_000388.2:p.Ile189Asn
|
|
XM_011543890.1:c.260T>A
|
XP_011542192.1:p.Ile87Asn
|
|
NM_000397.4:c.566T>A
MANE Select
|
NP_000388.2:p.Ile189Asn
|
|