ENST00000696170.1:c.*496C>A
|
ENSP00000512461.1:n.*496C>A
|
|
ENST00000696171.1:c.891C>A
|
ENSP00000512462.1:p.Cys297Ter
|
|
ENST00000378588.5:c.987C>A
MANE Select
|
ENSP00000367851.4:p.Cys329Ter
|
|
ENST00000378588.4:c.987C>A
|
ENSP00000367851.4:p.Cys329Ter
|
|
ENST00000465127.1:c.171+377966C>A
|
ENSP00000417050.1:n.171+377966C>A
|
|
ENST00000492288.1:n.412C>A
|
|
|
NM_000397.3:c.987C>A , LRG_53t1:c.987C>A
|
NP_000388.2:p.Cys329Ter
|
|
XM_011543890.1:c.681C>A
|
XP_011542192.1:p.Cys227Ter
|
|
NM_000397.4:c.987C>A
MANE Select
|
NP_000388.2:p.Cys329Ter
|
|