ENST00000592092.2:n.1437G>C
|
|
|
ENST00000673918.2:c.6977G>C
|
ENSP00000501283.1:p.Ser2326Thr
|
|
ENST00000674114.2:c.4584G>C
|
ENSP00000501039.2:n.4584G>C
|
|
ENST00000684977.1:c.2238G>C
|
ENSP00000509384.1:n.2238G>C
|
|
ENST00000689544.1:n.2284G>C
|
|
|
ENST00000691421.1:c.2181-83G>C
|
ENSP00000508674.1:n.2181-83G>C
|
|
ENST00000691855.1:c.6585G>C
|
|
|
ENST00000692961.1:c.6960-69G>C
|
ENSP00000509289.1:n.6960-69G>C
|
|
ENST00000693677.1:c.788G>C
|
ENSP00000509779.1:p.Ser263Thr
|
|
ENST00000420124.4:c.7043G>C
MANE Select
|
ENSP00000398837.2:p.Ser2348Thr
|
|
ENST00000673918.1:c.6977G>C
|
ENSP00000501283.1:p.Ser2326Thr
|
|
ENST00000674114.1:c.4365G>C
|
|
|
ENST00000420124.2:c.7043G>C
|
ENSP00000398837.1:p.Ser2348Thr
|
|
ENST00000592092.1:n.423G>C
|
|
|
NM_014727.2:c.7043G>C
|
NP_055542.1:p.Ser2348Thr
|
|
XM_011527561.1:c.6977G>C
|
XP_011525863.1:p.Ser2326Thr
|
|
XM_011527562.1:c.7043G>C
|
XP_011525864.1:p.Ser2348Thr
|
|
XM_011527563.1:c.6767G>C
|
XP_011525865.1:p.Ser2256Thr
|
|
XM_011527561.2:c.6479G>C
|
XP_011525863.2:p.Ser2160Thr
|
|
XM_011527562.2:c.7043G>C
|
XP_011525864.1:p.Ser2348Thr
|
|
XM_017027544.1:c.6960-83G>C
|
XP_016883033.1:n.6960-83G>C
|
|
XM_017027545.1:c.6479G>C
|
XP_016883034.1:p.Ser2160Thr
|
|
XM_017027546.1:c.4007G>C
|
XP_016883035.1:p.Ser1336Thr
|
|
NM_014727.3:c.7043G>C
MANE Select
|
NP_055542.1:p.Ser2348Thr
|
|