ENST00000261769.10:c.1759G>T
MANE Select
|
ENSP00000261769.4:p.Asp587Tyr
|
|
ENST00000261769.9:c.1759G>T
|
ENSP00000261769.4:p.Asp587Tyr
|
|
ENST00000422392.6:c.1576G>T
|
ENSP00000414946.2:p.Asp526Tyr
|
|
ENST00000562836.5:n.1830G>T
|
|
|
ENST00000566510.5:c.*425G>T
|
ENSP00000458139.1:n.*425G>T
|
|
ENST00000566612.5:c.1613G>T
|
ENSP00000454782.1:p.Ter538Leu
|
|
ENST00000611625.4:c.1822G>T
|
ENSP00000481063.1:p.Asp608Tyr
|
|
ENST00000612417.4:c.1759G>T
|
ENSP00000478360.1:p.Asp587Tyr
|
|
ENST00000621016.4:c.1759G>T
|
ENSP00000480664.1:p.Asp587Tyr
|
|
NM_004360.3:c.1759G>T , LRG_301t1:c.1759G>T
|
NP_004351.1:p.Asp587Tyr
|
|
XM_011523488.1:c.1024G>T
|
XP_011521790.1:p.Asp342Tyr
|
|
XM_011523489.1:c.1024G>T
|
XP_011521791.1:p.Asp342Tyr
|
|
NM_001317184.1:c.1576G>T
|
NP_001304113.1:p.Asp526Tyr
|
|
NM_001317185.1:c.211G>T
|
NP_001304114.1:p.Asp71Tyr
|
|
NM_001317186.1:c.-207G>T
|
NP_001304115.1:n.-207G>T
|
|
NM_004360.4:c.1759G>T
|
NP_004351.1:p.Asp587Tyr
|
|
NM_004360.5:c.1759G>T
MANE Select
|
NP_004351.1:p.Asp587Tyr
|
|
NM_001317184.2:c.1576G>T
|
NP_001304113.1:p.Asp526Tyr
|
|
NM_001317185.2:c.211G>T
|
NP_001304114.1:p.Asp71Tyr
|
|
NM_001317186.2:c.-207G>T
|
NP_001304115.1:n.-207G>T
|
|