ENST00000359842.10:c.416G>A
MANE Select
|
ENSP00000352900.5:p.Cys139Tyr
|
|
ENST00000359842.9:c.416G>A
|
ENSP00000352900.5:p.Cys139Tyr
|
|
ENST00000470566.1:n.341G>A
|
|
|
ENST00000619224.1:c.47G>A
|
ENSP00000482458.1:p.Cys16Tyr
|
|
NM_001256570.1:c.47G>A
|
NP_001243499.1:p.Cys16Tyr
|
|
NM_001256571.1:c.47G>A
|
NP_001243500.1:p.Cys16Tyr
|
|
NM_006917.4:c.416G>A
|
NP_008848.1:p.Cys139Tyr
|
|
NM_006917.5:c.416G>A
MANE Select
|
NP_008848.1:p.Cys139Tyr
|
|
NM_001256571.2:c.47G>A
|
NP_001243500.1:p.Cys16Tyr
|
|
NM_001256570.2:c.47G>A
|
NP_001243499.1:p.Cys16Tyr
|
|