ENST00000592092.2:n.274G>C
|
|
|
ENST00000673918.2:c.5902G>C
|
ENSP00000501283.1:p.Asp1968His
|
|
ENST00000674114.2:c.3509G>C
|
ENSP00000501039.2:n.3509G>C
|
|
ENST00000684977.1:c.1186G>C
|
ENSP00000509384.1:p.Asp396His
|
|
ENST00000689544.1:n.1121G>C
|
|
|
ENST00000691421.1:c.1189G>C
|
ENSP00000508674.1:p.Asp397His
|
|
ENST00000691855.1:c.5510G>C
|
|
|
ENST00000692961.1:c.5968G>C
|
ENSP00000509289.1:p.Asp1990His
|
|
ENST00000693677.1:c.704+188G>C
|
ENSP00000509779.1:n.704+188G>C
|
|
ENST00000420124.4:c.5968G>C
MANE Select
|
ENSP00000398837.2:p.Asp1990His
|
|
ENST00000673918.1:c.5902G>C
|
ENSP00000501283.1:p.Asp1968His
|
|
ENST00000674114.1:c.3290G>C
|
|
|
ENST00000420124.2:c.5968G>C
|
ENSP00000398837.1:p.Asp1990His
|
|
NM_014727.2:c.5968G>C
|
NP_055542.1:p.Asp1990His
|
|
XM_011527561.1:c.5902G>C
|
XP_011525863.1:p.Asp1968His
|
|
XM_011527562.1:c.5968G>C
|
XP_011525864.1:p.Asp1990His
|
|
XM_011527563.1:c.5692G>C
|
XP_011525865.1:p.Asp1898His
|
|
XM_011527561.2:c.5404G>C
|
XP_011525863.2:p.Asp1802His
|
|
XM_011527562.2:c.5968G>C
|
XP_011525864.1:p.Asp1990His
|
|
XM_017027544.1:c.5968G>C
|
XP_016883033.1:p.Asp1990His
|
|
XM_017027545.1:c.5404G>C
|
XP_016883034.1:p.Asp1802His
|
|
XM_017027546.1:c.2932G>C
|
XP_016883035.1:p.Asp978His
|
|
NM_014727.3:c.5968G>C
MANE Select
|
NP_055542.1:p.Asp1990His
|
|