ENST00000404085.7:c.552G>C
MANE Select
|
ENSP00000384008.3:p.Leu184Phe
|
|
ENST00000404261.9:c.552G>C
|
ENSP00000384753.6:p.Leu184Phe
|
|
ENST00000594072.6:c.552G>C
|
ENSP00000468845.4:p.Leu184Phe
|
|
ENST00000651416.1:n.769G>C
|
|
|
ENST00000652132.1:c.519G>C
|
ENSP00000498416.1:p.Leu173Phe
|
|
ENST00000394458.7:c.714G>C
|
ENSP00000377971.4:p.Leu238Phe
|
|
ENST00000404085.5:c.*451G>C
|
ENSP00000384008.2:n.*451G>C
|
|
ENST00000404261.8:c.714G>C
|
ENSP00000384753.5:p.Leu238Phe
|
|
ENST00000594072.5:c.714G>C
|
ENSP00000468845.3:p.Leu238Phe
|
|
ENST00000596626.1:n.665G>C
|
|
|
ENST00000598347.2:c.554G>C
|
|
|
NM_001278443.1:c.681G>C
|
NP_001265372.1:p.Leu227Phe
|
|
NM_001278444.1:c.714G>C
|
NP_001265373.1:p.Leu238Phe
|
|
NM_001278445.1:c.618G>C
|
NP_001265374.1:p.Leu206Phe
|
|
NM_152363.5:c.714G>C
|
NP_689576.5:p.Leu238Phe
|
|
NR_103530.1:n.828G>C
|
|
|
NM_001278443.2:c.519G>C
|
NP_001265372.2:p.Leu173Phe
|
|
NM_001278444.2:c.552G>C
|
NP_001265373.2:p.Leu184Phe
|
|
NM_001278445.2:c.510G>C
|
NP_001265374.2:p.Leu170Phe
|
|
NM_152363.6:c.552G>C
MANE Select
|
NP_689576.6:p.Leu184Phe
|
|
NR_103530.2:n.572G>C
|
|
|