ENST00000673918.2:c.4938G>T
|
ENSP00000501283.1:p.Arg1646=
|
|
ENST00000674114.2:c.2545G>T
|
ENSP00000501039.2:n.2545G>T
|
|
ENST00000684977.1:c.222G>T
|
ENSP00000509384.1:p.Arg74=
|
|
ENST00000685168.1:c.430G>T
|
|
|
ENST00000689544.1:n.157G>T
|
|
|
ENST00000691421.1:c.225G>T
|
ENSP00000508674.1:p.Arg75=
|
|
ENST00000691855.1:c.4546G>T
|
|
|
ENST00000692961.1:c.5004G>T
|
ENSP00000509289.1:p.Arg1668=
|
|
ENST00000420124.4:c.5004G>T
MANE Select
|
ENSP00000398837.2:p.Arg1668=
|
|
ENST00000673918.1:c.4938G>T
|
ENSP00000501283.1:p.Arg1646=
|
|
ENST00000674114.1:c.2326G>T
|
|
|
ENST00000420124.2:c.5004G>T
|
ENSP00000398837.1:p.Arg1668=
|
|
NM_014727.2:c.5004G>T
|
NP_055542.1:p.Arg1668=
|
|
XM_011527561.1:c.4938G>T
|
XP_011525863.1:p.Arg1646=
|
|
XM_011527562.1:c.5004G>T
|
XP_011525864.1:p.Arg1668=
|
|
XM_011527563.1:c.4728G>T
|
XP_011525865.1:p.Arg1576=
|
|
XM_011527561.2:c.4440G>T
|
XP_011525863.2:p.Arg1480=
|
|
XM_011527562.2:c.5004G>T
|
XP_011525864.1:p.Arg1668=
|
|
XM_017027544.1:c.5004G>T
|
XP_016883033.1:p.Arg1668=
|
|
XM_017027545.1:c.4440G>T
|
XP_016883034.1:p.Arg1480=
|
|
XM_017027546.1:c.1968G>T
|
XP_016883035.1:p.Arg656=
|
|
NM_014727.3:c.5004G>T
MANE Select
|
NP_055542.1:p.Arg1668=
|
|