ENST00000269159.8:c.490+3139T>C
MANE Select
|
ENSP00000269159.3:n.490+3139T>C
|
|
ENST00000269159.7:c.490+3139T>C
|
ENSP00000269159.3:n.490+3139T>C
|
|
ENST00000383376.9:c.*492-102T>C
|
ENSP00000372867.4:n.*492-102T>C
|
|
ENST00000586230.1:c.212+3139T>C
|
|
|
ENST00000588167.1:n.243+3139T>C
|
|
|
ENST00000588752.5:n.575+3139T>C
|
|
|
ENST00000588927.5:c.-78+3139T>C
|
ENSP00000464767.1:n.-78+3139T>C
|
|
ENST00000589238.5:c.-78+3139T>C
|
ENSP00000465416.1:n.-78+3139T>C
|
|
ENST00000590107.5:c.*132+3139T>C
|
ENSP00000466059.1:n.*132+3139T>C
|
|
ENST00000590138.1:c.*93+3139T>C
|
ENSP00000465938.1:n.*93+3139T>C
|
|
NM_014214.2:c.490+3139T>C
|
NP_055029.1:n.490+3139T>C
|
|
XM_011525659.1:c.442+3139T>C
|
XP_011523961.1:n.442+3139T>C
|
|
XM_011525660.1:c.418+3139T>C
|
XP_011523962.1:n.418+3139T>C
|
|
XM_011525661.1:c.130+3139T>C
|
XP_011523963.1:n.130+3139T>C
|
|
XM_011525659.3:c.442+3139T>C
|
XP_011523961.1:n.442+3139T>C
|
|
XM_011525661.3:c.130+3139T>C
|
XP_011523963.1:n.130+3139T>C
|
|
NM_014214.3:c.490+3139T>C
MANE Select
|
NP_055029.1:n.490+3139T>C
|
|