ENST00000592092.2:n.662A>T
|
|
|
ENST00000673918.2:c.6290A>T
|
ENSP00000501283.1:p.Lys2097Met
|
|
ENST00000674114.2:c.3897A>T
|
ENSP00000501039.2:n.3897A>T
|
|
ENST00000684977.1:c.1574A>T
|
ENSP00000509384.1:p.Lys525Met
|
|
ENST00000689544.1:n.1509A>T
|
|
|
ENST00000691421.1:c.1577A>T
|
ENSP00000508674.1:p.Lys526Met
|
|
ENST00000691855.1:c.5898A>T
|
|
|
ENST00000692961.1:c.6356A>T
|
ENSP00000509289.1:p.Lys2119Met
|
|
ENST00000693677.1:c.704+576A>T
|
ENSP00000509779.1:n.704+576A>T
|
|
ENST00000420124.4:c.6356A>T
MANE Select
|
ENSP00000398837.2:p.Lys2119Met
|
|
ENST00000673918.1:c.6290A>T
|
ENSP00000501283.1:p.Lys2097Met
|
|
ENST00000674114.1:c.3678A>T
|
|
|
ENST00000420124.2:c.6356A>T
|
ENSP00000398837.1:p.Lys2119Met
|
|
NM_014727.2:c.6356A>T
|
NP_055542.1:p.Lys2119Met
|
|
XM_011527561.1:c.6290A>T
|
XP_011525863.1:p.Lys2097Met
|
|
XM_011527562.1:c.6356A>T
|
XP_011525864.1:p.Lys2119Met
|
|
XM_011527563.1:c.6080A>T
|
XP_011525865.1:p.Lys2027Met
|
|
XM_011527561.2:c.5792A>T
|
XP_011525863.2:p.Lys1931Met
|
|
XM_011527562.2:c.6356A>T
|
XP_011525864.1:p.Lys2119Met
|
|
XM_017027544.1:c.6356A>T
|
XP_016883033.1:p.Lys2119Met
|
|
XM_017027545.1:c.5792A>T
|
XP_016883034.1:p.Lys1931Met
|
|
XM_017027546.1:c.3320A>T
|
XP_016883035.1:p.Lys1107Met
|
|
NM_014727.3:c.6356A>T
MANE Select
|
NP_055542.1:p.Lys2119Met
|
|