ENST00000320005.6:c.2104-77T>C
MANE Select
|
ENSP00000316605.5:n.2104-77T>C
|
|
ENST00000681546.1:n.1924-77T>C
|
|
|
ENST00000681746.1:c.*515-77T>C
|
ENSP00000505959.1:n.*515-77T>C
|
|
ENST00000320005.5:c.2104-77T>C
|
ENSP00000316605.5:n.2104-77T>C
|
|
ENST00000517327.5:c.276+2482T>C
|
ENSP00000428329.1:n.276+2482T>C
|
|
NM_019098.4:c.2104-77T>C
|
NP_061971.3:n.2104-77T>C
|
|
XM_011517138.1:c.1690-77T>C
|
XP_011515440.1:n.1690-77T>C
|
|
XM_011517138.2:c.1690-77T>C
|
XP_011515440.1:n.1690-77T>C
|
|
NM_019098.5:c.2104-77T>C
MANE Select
|
NP_061971.3:n.2104-77T>C
|
|