ENST00000696170.1:c.*567T>A
|
ENSP00000512461.1:n.*567T>A
|
|
ENST00000696171.1:c.962T>A
|
ENSP00000512462.1:p.Ile321Asn
|
|
ENST00000378588.5:c.1058T>A
MANE Select
|
ENSP00000367851.4:p.Ile353Asn
|
|
ENST00000378588.4:c.1058T>A
|
ENSP00000367851.4:p.Ile353Asn
|
|
ENST00000465127.1:c.171+378037T>A
|
ENSP00000417050.1:n.171+378037T>A
|
|
ENST00000492288.1:n.483T>A
|
|
|
NM_000397.3:c.1058T>A , LRG_53t1:c.1058T>A
|
NP_000388.2:p.Ile353Asn
|
|
XM_011543890.1:c.752T>A
|
XP_011542192.1:p.Ile251Asn
|
|
NM_000397.4:c.1058T>A
MANE Select
|
NP_000388.2:p.Ile353Asn
|
|