ENST00000592092.2:n.259G>T
|
|
|
ENST00000673918.2:c.5887G>T
|
ENSP00000501283.1:p.Gly1963Ter
|
|
ENST00000674114.2:c.3494G>T
|
ENSP00000501039.2:n.3494G>T
|
|
ENST00000684977.1:c.1171G>T
|
ENSP00000509384.1:p.Gly391Ter
|
|
ENST00000689544.1:n.1106G>T
|
|
|
ENST00000691421.1:c.1174G>T
|
ENSP00000508674.1:p.Gly392Ter
|
|
ENST00000691855.1:c.5495G>T
|
|
|
ENST00000692961.1:c.5953G>T
|
ENSP00000509289.1:p.Gly1985Ter
|
|
ENST00000693677.1:c.704+173G>T
|
ENSP00000509779.1:n.704+173G>T
|
|
ENST00000420124.4:c.5953G>T
MANE Select
|
ENSP00000398837.2:p.Gly1985Ter
|
|
ENST00000673918.1:c.5887G>T
|
ENSP00000501283.1:p.Gly1963Ter
|
|
ENST00000674114.1:c.3275G>T
|
|
|
ENST00000420124.2:c.5953G>T
|
ENSP00000398837.1:p.Gly1985Ter
|
|
NM_014727.2:c.5953G>T
|
NP_055542.1:p.Gly1985Ter
|
|
XM_011527561.1:c.5887G>T
|
XP_011525863.1:p.Gly1963Ter
|
|
XM_011527562.1:c.5953G>T
|
XP_011525864.1:p.Gly1985Ter
|
|
XM_011527563.1:c.5677G>T
|
XP_011525865.1:p.Gly1893Ter
|
|
XM_011527561.2:c.5389G>T
|
XP_011525863.2:p.Gly1797Ter
|
|
XM_011527562.2:c.5953G>T
|
XP_011525864.1:p.Gly1985Ter
|
|
XM_017027544.1:c.5953G>T
|
XP_016883033.1:p.Gly1985Ter
|
|
XM_017027545.1:c.5389G>T
|
XP_016883034.1:p.Gly1797Ter
|
|
XM_017027546.1:c.2917G>T
|
XP_016883035.1:p.Gly973Ter
|
|
NM_014727.3:c.5953G>T
MANE Select
|
NP_055542.1:p.Gly1985Ter
|
|