ENST00000614874.2:c.476-169G>T
|
ENSP00000507272.1:n.476-169G>T
|
|
ENST00000682620.1:n.1631-169G>T
|
|
|
ENST00000684771.1:n.585-169G>T
|
|
|
ENST00000228872.9:c.476-169G>T
MANE Select
|
ENSP00000228872.4:n.476-169G>T
|
|
ENST00000228872.8:c.476-169G>T
|
ENSP00000228872.4:n.476-169G>T
|
|
ENST00000396340.1:c.475+342G>T
|
ENSP00000379629.1:n.475+342G>T
|
|
ENST00000442489.1:c.194-169G>T
|
ENSP00000407597.1:n.194-169G>T
|
|
ENST00000477087.1:n.155-169G>T
|
|
|
NM_004064.4:c.476-169G>T
|
NP_004055.1:n.476-169G>T
|
|
NM_004064.5:c.476-169G>T
MANE Select
|
NP_004055.1:n.476-169G>T
|
|