ENST00000404085.7:c.627T>A
MANE Select
|
ENSP00000384008.3:p.Pro209=
|
|
ENST00000404261.9:c.627T>A
|
ENSP00000384753.6:p.Pro209=
|
|
ENST00000594072.6:c.627T>A
|
ENSP00000468845.4:p.Pro209=
|
|
ENST00000651416.1:n.844T>A
|
|
|
ENST00000652132.1:c.594T>A
|
ENSP00000498416.1:p.Pro198=
|
|
ENST00000394458.7:c.789T>A
|
ENSP00000377971.4:p.Pro263=
|
|
ENST00000404085.5:c.*526T>A
|
ENSP00000384008.2:n.*526T>A
|
|
ENST00000404261.8:c.789T>A
|
ENSP00000384753.5:p.Pro263=
|
|
ENST00000594072.5:c.789T>A
|
ENSP00000468845.3:p.Pro263=
|
|
ENST00000596626.1:n.740T>A
|
|
|
ENST00000598347.2:c.629T>A
|
|
|
NM_001278443.1:c.756T>A
|
NP_001265372.1:p.Pro252=
|
|
NM_001278444.1:c.789T>A
|
NP_001265373.1:p.Pro263=
|
|
NM_001278445.1:c.693T>A
|
NP_001265374.1:p.Pro231=
|
|
NM_152363.5:c.789T>A
|
NP_689576.5:p.Pro263=
|
|
NR_103530.1:n.903T>A
|
|
|
NM_001278443.2:c.594T>A
|
NP_001265372.2:p.Pro198=
|
|
NM_001278444.2:c.627T>A
|
NP_001265373.2:p.Pro209=
|
|
NM_001278445.2:c.585T>A
|
NP_001265374.2:p.Pro195=
|
|
NM_152363.6:c.627T>A
MANE Select
|
NP_689576.6:p.Pro209=
|
|
NR_103530.2:n.647T>A
|
|
|