|
ENST00000261769.10:c.*1G>A
MANE Select
|
ENSP00000261769.4:n.*1G>A
|
|
|
ENST00000261769.9:c.*1G>A
|
ENSP00000261769.4:n.*1G>A
|
|
|
ENST00000422392.6:c.*1G>A
|
ENSP00000414946.2:n.*1G>A
|
|
|
ENST00000562118.1:n.868G>A
|
|
|
|
ENST00000562836.5:n.2721G>A
|
|
|
|
ENST00000566510.5:c.*1316G>A
|
ENSP00000458139.1:n.*1316G>A
|
|
|
ENST00000566612.5:c.*890G>A
|
ENSP00000454782.1:n.*890G>A
|
|
|
ENST00000611625.4:c.*1G>A
|
ENSP00000481063.1:n.*1G>A
|
|
|
ENST00000612417.4:c.1854-691G>A
|
ENSP00000478360.1:n.1854-691G>A
|
|
|
ENST00000621016.4:c.1866-703G>A
|
ENSP00000480664.1:n.1866-703G>A
|
|
|
NM_004360.3:c.*1G>A , LRG_301t1:c.*1G>A
|
NP_004351.1:n.*1G>A
|
|
|
XM_011523488.1:c.*1G>A
|
XP_011521790.1:n.*1G>A
|
|
|
XM_011523489.1:c.*1G>A
|
XP_011521791.1:n.*1G>A
|
|
|
NM_001317184.1:c.*1G>A
|
NP_001304113.1:n.*1G>A
|
|
|
NM_001317185.1:c.*1G>A
|
NP_001304114.1:n.*1G>A
|
|
|
NM_001317186.1:c.*1G>A
|
NP_001304115.1:n.*1G>A
|
|
|
NM_004360.4:c.*1G>A
|
NP_004351.1:n.*1G>A
|
|
|
NM_004360.5:c.*1G>A
MANE Select
|
NP_004351.1:n.*1G>A
|
|
|
NM_001317184.2:c.*1G>A
|
NP_001304113.1:n.*1G>A
|
|
|
NM_001317185.2:c.*1G>A
|
NP_001304114.1:n.*1G>A
|
|
|
NM_001317186.2:c.*1G>A
|
NP_001304115.1:n.*1G>A
|
|
