ENST00000696170.1:c.*573T>G
|
ENSP00000512461.1:n.*573T>G
|
|
ENST00000696171.1:c.968T>G
|
ENSP00000512462.1:p.Ile323Ser
|
|
ENST00000378588.5:c.1064T>G
MANE Select
|
ENSP00000367851.4:p.Ile355Ser
|
|
ENST00000378588.4:c.1064T>G
|
ENSP00000367851.4:p.Ile355Ser
|
|
ENST00000465127.1:c.171+378043T>G
|
ENSP00000417050.1:n.171+378043T>G
|
|
ENST00000492288.1:n.489T>G
|
|
|
NM_000397.3:c.1064T>G , LRG_53t1:c.1064T>G
|
NP_000388.2:p.Ile355Ser
|
|
XM_011543890.1:c.758T>G
|
XP_011542192.1:p.Ile253Ser
|
|
NM_000397.4:c.1064T>G
MANE Select
|
NP_000388.2:p.Ile355Ser
|
|