ENST00000592092.2:n.965T>C
|
|
|
ENST00000673918.2:c.6593T>C
|
ENSP00000501283.1:p.Leu2198Ser
|
|
ENST00000674114.2:c.4200T>C
|
ENSP00000501039.2:n.4200T>C
|
|
ENST00000684977.1:c.1877T>C
|
ENSP00000509384.1:p.Leu626Ser
|
|
ENST00000689544.1:n.1812T>C
|
|
|
ENST00000691421.1:c.1880T>C
|
ENSP00000508674.1:p.Leu627Ser
|
|
ENST00000691855.1:c.6201T>C
|
|
|
ENST00000692961.1:c.6659T>C
|
ENSP00000509289.1:p.Leu2220Ser
|
|
ENST00000693677.1:c.705-389T>C
|
ENSP00000509779.1:n.705-389T>C
|
|
ENST00000420124.4:c.6659T>C
MANE Select
|
ENSP00000398837.2:p.Leu2220Ser
|
|
ENST00000673918.1:c.6593T>C
|
ENSP00000501283.1:p.Leu2198Ser
|
|
ENST00000674114.1:c.3981T>C
|
|
|
ENST00000420124.2:c.6659T>C
|
ENSP00000398837.1:p.Leu2220Ser
|
|
NM_014727.2:c.6659T>C
|
NP_055542.1:p.Leu2220Ser
|
|
XM_011527561.1:c.6593T>C
|
XP_011525863.1:p.Leu2198Ser
|
|
XM_011527562.1:c.6659T>C
|
XP_011525864.1:p.Leu2220Ser
|
|
XM_011527563.1:c.6383T>C
|
XP_011525865.1:p.Leu2128Ser
|
|
XM_011527561.2:c.6095T>C
|
XP_011525863.2:p.Leu2032Ser
|
|
XM_011527562.2:c.6659T>C
|
XP_011525864.1:p.Leu2220Ser
|
|
XM_017027544.1:c.6659T>C
|
XP_016883033.1:p.Leu2220Ser
|
|
XM_017027545.1:c.6095T>C
|
XP_016883034.1:p.Leu2032Ser
|
|
XM_017027546.1:c.3623T>C
|
XP_016883035.1:p.Leu1208Ser
|
|
NM_014727.3:c.6659T>C
MANE Select
|
NP_055542.1:p.Leu2220Ser
|
|