ENST00000261769.10:c.2084G>A
MANE Select
|
ENSP00000261769.4:p.Cys695Tyr
|
|
ENST00000261769.9:c.2084G>A
|
ENSP00000261769.4:p.Cys695Tyr
|
|
ENST00000422392.6:c.1901G>A
|
ENSP00000414946.2:p.Cys634Tyr
|
|
ENST00000562118.1:n.302G>A
|
|
|
ENST00000562836.5:n.2155G>A
|
|
|
ENST00000566510.5:c.*750G>A
|
ENSP00000458139.1:n.*750G>A
|
|
ENST00000566612.5:c.*324G>A
|
ENSP00000454782.1:n.*324G>A
|
|
ENST00000611625.4:c.2147G>A
|
ENSP00000481063.1:p.Cys716Tyr
|
|
ENST00000612417.4:c.1830+1427G>A
|
ENSP00000478360.1:n.1830+1427G>A
|
|
ENST00000621016.4:c.1865+1392G>A
|
ENSP00000480664.1:n.1865+1392G>A
|
|
NM_004360.3:c.2084G>A , LRG_301t1:c.2084G>A
|
NP_004351.1:p.Cys695Tyr
|
|
XM_011523488.1:c.1349G>A
|
XP_011521790.1:p.Cys450Tyr
|
|
XM_011523489.1:c.1349G>A
|
XP_011521791.1:p.Cys450Tyr
|
|
NM_001317184.1:c.1901G>A
|
NP_001304113.1:p.Cys634Tyr
|
|
NM_001317185.1:c.536G>A
|
NP_001304114.1:p.Cys179Tyr
|
|
NM_001317186.1:c.119G>A
|
NP_001304115.1:p.Cys40Tyr
|
|
NM_004360.4:c.2084G>A
|
NP_004351.1:p.Cys695Tyr
|
|
NM_004360.5:c.2084G>A
MANE Select
|
NP_004351.1:p.Cys695Tyr
|
|
NM_001317184.2:c.1901G>A
|
NP_001304113.1:p.Cys634Tyr
|
|
NM_001317185.2:c.536G>A
|
NP_001304114.1:p.Cys179Tyr
|
|
NM_001317186.2:c.119G>A
|
NP_001304115.1:p.Cys40Tyr
|
|