ENST00000404085.7:c.588C>G
MANE Select
|
ENSP00000384008.3:p.Pro196=
|
|
ENST00000404261.9:c.588C>G
|
ENSP00000384753.6:p.Pro196=
|
|
ENST00000594072.6:c.588C>G
|
ENSP00000468845.4:p.Pro196=
|
|
ENST00000651416.1:n.805C>G
|
|
|
ENST00000652132.1:c.555C>G
|
ENSP00000498416.1:p.Pro185=
|
|
ENST00000394458.7:c.750C>G
|
ENSP00000377971.4:p.Pro250=
|
|
ENST00000404085.5:c.*487C>G
|
ENSP00000384008.2:n.*487C>G
|
|
ENST00000404261.8:c.750C>G
|
ENSP00000384753.5:p.Pro250=
|
|
ENST00000594072.5:c.750C>G
|
ENSP00000468845.3:p.Pro250=
|
|
ENST00000596626.1:n.701C>G
|
|
|
ENST00000598347.2:c.590C>G
|
|
|
NM_001278443.1:c.717C>G
|
NP_001265372.1:p.Pro239=
|
|
NM_001278444.1:c.750C>G
|
NP_001265373.1:p.Pro250=
|
|
NM_001278445.1:c.654C>G
|
NP_001265374.1:p.Pro218=
|
|
NM_152363.5:c.750C>G
|
NP_689576.5:p.Pro250=
|
|
NR_103530.1:n.864C>G
|
|
|
NM_001278443.2:c.555C>G
|
NP_001265372.2:p.Pro185=
|
|
NM_001278444.2:c.588C>G
|
NP_001265373.2:p.Pro196=
|
|
NM_001278445.2:c.546C>G
|
NP_001265374.2:p.Pro182=
|
|
NM_152363.6:c.588C>G
MANE Select
|
NP_689576.6:p.Pro196=
|
|
NR_103530.2:n.608C>G
|
|
|