ENST00000266087.12:c.645+292T>C
MANE Select
|
ENSP00000266087.7:n.645+292T>C
|
|
ENST00000266087.11:c.645+292T>C
|
ENSP00000266087.7:n.645+292T>C
|
|
ENST00000397426.5:c.303+292T>C
|
ENSP00000380571.1:n.303+292T>C
|
|
ENST00000420700.5:c.*224+292T>C
|
ENSP00000406155.1:n.*224+292T>C
|
|
ENST00000425028.5:c.*343+292T>C
|
ENSP00000395823.1:n.*343+292T>C
|
|
ENST00000452138.3:c.408+292T>C
|
ENSP00000388547.2:n.408+292T>C
|
|
ENST00000492535.1:n.481+292T>C
|
|
|
NM_001033024.1:c.408+292T>C
|
NP_001028196.1:n.408+292T>C
|
|
NM_001257990.1:c.303+292T>C
|
NP_001244919.1:n.303+292T>C
|
|
NM_012179.3:c.645+292T>C
|
NP_036311.3:n.645+292T>C
|
|
XM_011530106.1:c.177+292T>C
|
XP_011528408.1:n.177+292T>C
|
|
XM_024452207.1:c.303+292T>C
|
XP_024307975.1:n.303+292T>C
|
|
NM_012179.4:c.645+292T>C
MANE Select
|
NP_036311.3:n.645+292T>C
|
|
NM_001033024.2:c.408+292T>C
|
NP_001028196.1:n.408+292T>C
|
|
NM_001257990.2:c.303+292T>C
|
NP_001244919.1:n.303+292T>C
|
|