ENST00000673918.2:c.5005G>T
|
ENSP00000501283.1:p.Gly1669Cys
|
|
ENST00000674114.2:c.2612G>T
|
ENSP00000501039.2:n.2612G>T
|
|
ENST00000684977.1:c.289G>T
|
ENSP00000509384.1:p.Gly97Cys
|
|
ENST00000685168.1:c.497G>T
|
|
|
ENST00000689544.1:n.224G>T
|
|
|
ENST00000691421.1:c.292G>T
|
ENSP00000508674.1:p.Gly98Cys
|
|
ENST00000691855.1:c.4613G>T
|
|
|
ENST00000692961.1:c.5071G>T
|
ENSP00000509289.1:p.Gly1691Cys
|
|
ENST00000420124.4:c.5071G>T
MANE Select
|
ENSP00000398837.2:p.Gly1691Cys
|
|
ENST00000673918.1:c.5005G>T
|
ENSP00000501283.1:p.Gly1669Cys
|
|
ENST00000674114.1:c.2393G>T
|
|
|
ENST00000420124.2:c.5071G>T
|
ENSP00000398837.1:p.Gly1691Cys
|
|
NM_014727.2:c.5071G>T
|
NP_055542.1:p.Gly1691Cys
|
|
XM_011527561.1:c.5005G>T
|
XP_011525863.1:p.Gly1669Cys
|
|
XM_011527562.1:c.5071G>T
|
XP_011525864.1:p.Gly1691Cys
|
|
XM_011527563.1:c.4795G>T
|
XP_011525865.1:p.Gly1599Cys
|
|
XM_011527561.2:c.4507G>T
|
XP_011525863.2:p.Gly1503Cys
|
|
XM_011527562.2:c.5071G>T
|
XP_011525864.1:p.Gly1691Cys
|
|
XM_017027544.1:c.5071G>T
|
XP_016883033.1:p.Gly1691Cys
|
|
XM_017027545.1:c.4507G>T
|
XP_016883034.1:p.Gly1503Cys
|
|
XM_017027546.1:c.2035G>T
|
XP_016883035.1:p.Gly679Cys
|
|
NM_014727.3:c.5071G>T
MANE Select
|
NP_055542.1:p.Gly1691Cys
|
|