ENST00000696170.1:c.218del
|
ENSP00000512461.1:p.Arg73GlnfsTer?
|
|
ENST00000696171.1:c.122del
|
ENSP00000512462.1:p.Arg41GlnfsTer?
|
|
ENST00000696172.1:c.218del
|
ENSP00000512463.1:p.Arg73GlnfsTer?
|
|
ENST00000696173.1:n.226del
|
|
|
ENST00000378588.5:c.218del
MANE Select
|
ENSP00000367851.4:p.Arg73GlnfsTer?
|
|
ENST00000378588.4:c.218del
|
ENSP00000367851.4:p.Arg73GlnfsTer?
|
|
ENST00000465127.1:c.171+357566del
|
ENSP00000417050.1:n.171+357566del
|
|
NM_000397.3:c.218del , LRG_53t1:c.218del
|
NP_000388.2:p.Arg73GlnfsTer?
|
|
XM_011543890.1:c.-213del
|
XP_011542192.1:n.-213del
|
|
NM_000397.4:c.218del
MANE Select
|
NP_000388.2:p.Arg73GlnfsTer?
|
|