ENST00000592092.2:n.571G>T
|
|
|
ENST00000673918.2:c.6199G>T
|
ENSP00000501283.1:p.Gly2067Ter
|
|
ENST00000674114.2:c.3806G>T
|
ENSP00000501039.2:n.3806G>T
|
|
ENST00000684977.1:c.1483G>T
|
ENSP00000509384.1:p.Gly495Ter
|
|
ENST00000689544.1:n.1418G>T
|
|
|
ENST00000691421.1:c.1486G>T
|
ENSP00000508674.1:p.Gly496Ter
|
|
ENST00000691855.1:c.5807G>T
|
|
|
ENST00000692961.1:c.6265G>T
|
ENSP00000509289.1:p.Gly2089Ter
|
|
ENST00000693677.1:c.704+485G>T
|
ENSP00000509779.1:n.704+485G>T
|
|
ENST00000420124.4:c.6265G>T
MANE Select
|
ENSP00000398837.2:p.Gly2089Ter
|
|
ENST00000673918.1:c.6199G>T
|
ENSP00000501283.1:p.Gly2067Ter
|
|
ENST00000674114.1:c.3587G>T
|
|
|
ENST00000420124.2:c.6265G>T
|
ENSP00000398837.1:p.Gly2089Ter
|
|
NM_014727.2:c.6265G>T
|
NP_055542.1:p.Gly2089Ter
|
|
XM_011527561.1:c.6199G>T
|
XP_011525863.1:p.Gly2067Ter
|
|
XM_011527562.1:c.6265G>T
|
XP_011525864.1:p.Gly2089Ter
|
|
XM_011527563.1:c.5989G>T
|
XP_011525865.1:p.Gly1997Ter
|
|
XM_011527561.2:c.5701G>T
|
XP_011525863.2:p.Gly1901Ter
|
|
XM_011527562.2:c.6265G>T
|
XP_011525864.1:p.Gly2089Ter
|
|
XM_017027544.1:c.6265G>T
|
XP_016883033.1:p.Gly2089Ter
|
|
XM_017027545.1:c.5701G>T
|
XP_016883034.1:p.Gly1901Ter
|
|
XM_017027546.1:c.3229G>T
|
XP_016883035.1:p.Gly1077Ter
|
|
NM_014727.3:c.6265G>T
MANE Select
|
NP_055542.1:p.Gly2089Ter
|
|