ENST00000576742.6:c.1676G>C
MANE Select
|
ENSP00000461518.2:p.Trp559Ser
|
|
ENST00000301365.8:c.1676G>C
|
ENSP00000301365.4:p.Trp559Ser
|
|
ENST00000381913.8:c.938G>C
|
|
|
ENST00000571139.5:c.*1668G>C
|
ENSP00000458187.1:n.*1668G>C
|
|
ENST00000572519.1:c.1676G>C
|
ENSP00000460215.1:p.Trp559Ser
|
|
ENST00000573539.5:c.*1686G>C
|
ENSP00000458239.1:n.*1686G>C
|
|
ENST00000576742.5:c.1676G>C
|
ENSP00000461518.1:p.Trp559Ser
|
|
ENST00000577016.5:c.328+2589G>C
|
|
|
ENST00000616411.4:c.1628G>C
|
ENSP00000483947.1:p.Trp543Ser
|
|
NM_001258205.1:c.1676G>C
|
NP_001245134.1:p.Trp559Ser
|
|
NM_145068.3:c.1676G>C
|
NP_659505.1:p.Trp559Ser
|
|
XM_011523693.1:c.1577+2589G>C
|
XP_011521995.1:n.1577+2589G>C
|
|
XM_011523694.1:c.971G>C
|
XP_011521996.1:p.Trp324Ser
|
|
XM_011523695.1:c.629G>C
|
XP_011521997.1:p.Trp210Ser
|
|
XR_934004.1:n.1750G>C
|
|
|
NM_001258205.2:c.1676G>C
|
NP_001245134.1:p.Trp559Ser
|
|
NM_145068.4:c.1676G>C
MANE Select
|
NP_659505.1:p.Trp559Ser
|
|