ENST00000409134.8:c.*268T>C
MANE Select
|
ENSP00000387123.3:n.*268T>C
|
|
ENST00000635851.1:c.1563+1627T>C
|
|
|
ENST00000636743.1:c.*268T>C
|
ENSP00000489725.1:n.*268T>C
|
|
ENST00000636808.1:c.*1697T>C
|
ENSP00000490833.1:n.*1697T>C
|
|
ENST00000636872.1:c.2048T>C
|
ENSP00000490919.1:n.2048T>C
|
|
ENST00000636879.1:c.*268T>C
|
ENSP00000490811.1:n.*268T>C
|
|
ENST00000636886.1:c.*268T>C
|
ENSP00000490371.1:n.*268T>C
|
|
ENST00000637206.1:c.*268T>C
|
ENSP00000489895.1:n.*268T>C
|
|
ENST00000637272.1:c.*268T>C
|
ENSP00000489686.1:n.*268T>C
|
|
ENST00000637782.1:c.1565+1627T>C
|
ENSP00000490024.1:n.1565+1627T>C
|
|
ENST00000409134.7:c.*268T>C
|
ENSP00000387123.3:n.*268T>C
|
|
ENST00000447989.6:c.*268T>C
|
ENSP00000414132.2:n.*268T>C
|
|
ENST00000553117.5:c.*268T>C
|
ENSP00000448593.1:n.*268T>C
|
|
NM_001182.4:c.*268T>C
|
NP_001173.2:n.*268T>C
|
|
NM_001201377.1:c.*268T>C
|
NP_001188306.1:n.*268T>C
|
|
NM_001202404.1:c.*268T>C
|
NP_001189333.1:n.*268T>C
|
|
XM_011543417.2:c.*268T>C
|
XP_011541719.1:n.*268T>C
|
|
NM_001182.5:c.*268T>C
MANE Select
|
NP_001173.2:n.*268T>C
|
|
NM_001201377.2:c.*268T>C
|
NP_001188306.1:n.*268T>C
|
|
NM_001202404.2:c.*268T>C
|
NP_001189333.2:n.*268T>C
|
|