ENST00000592092.2:n.801G>C
|
|
|
ENST00000673918.2:c.6429G>C
|
ENSP00000501283.1:p.Trp2143Cys
|
|
ENST00000674114.2:c.4036G>C
|
ENSP00000501039.2:n.4036G>C
|
|
ENST00000684977.1:c.1713G>C
|
ENSP00000509384.1:p.Trp571Cys
|
|
ENST00000689544.1:n.1648G>C
|
|
|
ENST00000691421.1:c.1716G>C
|
ENSP00000508674.1:p.Trp572Cys
|
|
ENST00000691855.1:c.6037G>C
|
|
|
ENST00000692961.1:c.6495G>C
|
ENSP00000509289.1:p.Trp2165Cys
|
|
ENST00000693677.1:c.705-553G>C
|
ENSP00000509779.1:n.705-553G>C
|
|
ENST00000420124.4:c.6495G>C
MANE Select
|
ENSP00000398837.2:p.Trp2165Cys
|
|
ENST00000673918.1:c.6429G>C
|
ENSP00000501283.1:p.Trp2143Cys
|
|
ENST00000674114.1:c.3817G>C
|
|
|
ENST00000420124.2:c.6495G>C
|
ENSP00000398837.1:p.Trp2165Cys
|
|
NM_014727.2:c.6495G>C
|
NP_055542.1:p.Trp2165Cys
|
|
XM_011527561.1:c.6429G>C
|
XP_011525863.1:p.Trp2143Cys
|
|
XM_011527562.1:c.6495G>C
|
XP_011525864.1:p.Trp2165Cys
|
|
XM_011527563.1:c.6219G>C
|
XP_011525865.1:p.Trp2073Cys
|
|
XM_011527561.2:c.5931G>C
|
XP_011525863.2:p.Trp1977Cys
|
|
XM_011527562.2:c.6495G>C
|
XP_011525864.1:p.Trp2165Cys
|
|
XM_017027544.1:c.6495G>C
|
XP_016883033.1:p.Trp2165Cys
|
|
XM_017027545.1:c.5931G>C
|
XP_016883034.1:p.Trp1977Cys
|
|
XM_017027546.1:c.3459G>C
|
XP_016883035.1:p.Trp1153Cys
|
|
NM_014727.3:c.6495G>C
MANE Select
|
NP_055542.1:p.Trp2165Cys
|
|