ENST00000222572.8:c.-16G>C
MANE Select
|
ENSP00000222572.3:n.-16G>C
|
|
ENST00000222572.7:c.-16G>C
|
ENSP00000222572.3:n.-16G>C
|
|
ENST00000433091.6:c.-16G>C
|
ENSP00000404622.2:n.-16G>C
|
|
ENST00000446142.5:c.-16G>C
|
ENSP00000405211.1:n.-16G>C
|
|
ENST00000455123.5:c.-16G>C
|
ENSP00000414515.1:n.-16G>C
|
|
ENST00000469716.1:n.62G>C
|
|
|
ENST00000469926.5:c.-273G>C
|
ENSP00000488550.1:n.-273G>C
|
|
ENST00000471883.1:n.64G>C
|
|
|
ENST00000490778.5:c.-328G>C
|
ENSP00000488826.1:n.-328G>C
|
|
ENST00000493290.5:c.-349G>C
|
ENSP00000488822.1:n.-349G>C
|
|
ENST00000632034.1:c.-16G>C
|
ENSP00000487898.1:n.-16G>C
|
|
ENST00000633192.1:c.48G>C
|
ENSP00000488378.1:p.Ala16=
|
|
ENST00000633531.1:c.-16G>C
|
ENSP00000488838.1:n.-16G>C
|
|
NM_000305.2:c.-16G>C
|
NP_000296.2:n.-16G>C
|
|
NM_001018161.1:c.-16G>C
|
NP_001018171.1:n.-16G>C
|
|
XM_005250453.1:c.-194G>C
|
XP_005250510.1:n.-194G>C
|
|
XM_005250454.1:c.-270G>C
|
XP_005250511.1:n.-270G>C
|
|
XM_011516333.1:c.-344G>C
|
XP_011514635.1:n.-344G>C
|
|
XM_017012357.2:c.-270G>C
|
XP_016867846.1:n.-270G>C
|
|
XM_017012358.2:c.-344G>C
|
XP_016867847.1:n.-344G>C
|
|
NM_000305.3:c.-16G>C
MANE Select
|
NP_000296.2:n.-16G>C
|
|
NM_001018161.2:c.-16G>C
|
NP_001018171.1:n.-16G>C
|
|