|
ENST00000409134.8:c.1534G>T
MANE Select
|
ENSP00000387123.3:p.Ala512Ser
|
|
|
ENST00000458249.6:c.*1443G>T
|
ENSP00000403929.1:n.*1443G>T
|
|
|
ENST00000485852.7:n.281G>T
|
|
|
|
ENST00000497231.7:n.1961G>T
|
|
|
|
ENST00000635851.1:c.1532G>T
|
|
|
|
ENST00000636225.1:c.*1478G>T
|
ENSP00000490797.1:n.*1478G>T
|
|
|
ENST00000636286.1:n.1299G>T
|
|
|
|
ENST00000636482.1:n.1068G>T
|
|
|
|
ENST00000636743.1:c.1414G>T
|
ENSP00000489725.1:p.Ala472Ser
|
|
|
ENST00000636808.1:c.*1343G>T
|
ENSP00000490833.1:n.*1343G>T
|
|
|
ENST00000636872.1:c.1694G>T
|
ENSP00000490919.1:n.1694G>T
|
|
|
ENST00000636879.1:c.1579G>T
|
ENSP00000490811.1:p.Ala527Ser
|
|
|
ENST00000636886.1:c.1333G>T
|
ENSP00000490371.1:p.Ala445Ser
|
|
|
ENST00000637206.1:c.1354G>T
|
ENSP00000489895.1:p.Ala452Ser
|
|
|
ENST00000637272.1:c.1525G>T
|
ENSP00000489686.1:p.Ala509Ser
|
|
|
ENST00000637292.1:c.990G>T
|
|
|
|
ENST00000637782.1:c.1534G>T
|
ENSP00000490024.1:p.Ala512Ser
|
|
|
ENST00000638008.1:c.*1378G>T
|
ENSP00000490400.1:n.*1378G>T
|
|
|
ENST00000638010.1:n.1480G>T
|
|
|
|
ENST00000409134.7:c.1534G>T
|
ENSP00000387123.3:p.Ala512Ser
|
|
|
ENST00000447989.6:c.1423G>T
|
ENSP00000414132.2:p.Ala475Ser
|
|
|
ENST00000485852.6:n.281G>T
|
|
|
|
ENST00000497231.6:n.1744G>T
|
|
|
|
ENST00000553117.5:c.1342G>T
|
ENSP00000448593.1:p.Ala448Ser
|
|
|
NM_001182.4:c.1534G>T
|
NP_001173.2:p.Ala512Ser
|
|
|
NM_001201377.1:c.1450G>T
|
NP_001188306.1:p.Ala484Ser
|
|
|
NM_001202404.1:c.1423G>T
|
NP_001189333.1:p.Ala475Ser
|
|
|
XM_011543417.1:c.1129G>T
|
XP_011541719.1:p.Ala377Ser
|
|
|
XM_011543417.2:c.1129G>T
|
XP_011541719.1:p.Ala377Ser
|
|
|
NM_001182.5:c.1534G>T
MANE Select
|
NP_001173.2:p.Ala512Ser
|
|
|
NM_001201377.2:c.1450G>T
|
NP_001188306.1:p.Ala484Ser
|
|
|
NM_001202404.2:c.1342G>T
|
NP_001189333.2:p.Ala448Ser
|
|
