ENST00000699620.1:c.-441T=
|
ENSP00000514480.1:n.-441T=
|
|
ENST00000699640.1:c.-385+1325T=
|
ENSP00000514493.1:n.-385+1325T=
|
|
ENST00000367057.8:c.2T=
MANE Select
|
ENSP00000356024.3:p.Met1=
|
|
ENST00000367057.7:c.2T=
|
ENSP00000356024.3:p.Met1=
|
|
ENST00000367058.7:c.2T=
|
ENSP00000356025.3:p.Met1=
|
|
ENST00000367059.3:c.2T=
|
ENSP00000356026.3:p.Met1=
|
|
NM_001006658.2:c.2T= , LRG_348t1:c.2T=
|
NP_001006659.1:p.Met1=
|
|
NM_001877.4:c.2T=
|
NP_001868.2:p.Met1=
|
|
NM_001006658.3:c.2T=
MANE Select
|
NP_001006659.1:p.Met1=
|
|
NM_001877.5:c.2T=
|
NP_001868.2:p.Met1=
|
|