ENST00000614874.2:c.*1198A>T
|
ENSP00000507272.1:n.*1198A>T
|
|
ENST00000682620.1:n.1761-892A>T
|
|
|
ENST00000684771.1:n.715-892A>T
|
|
|
ENST00000228872.9:c.*9-892A>T
MANE Select
|
ENSP00000228872.4:n.*9-892A>T
|
|
ENST00000228872.8:c.*9-892A>T
|
ENSP00000228872.4:n.*9-892A>T
|
|
ENST00000396340.1:c.476-921A>T
|
ENSP00000379629.1:n.476-921A>T
|
|
ENST00000442489.1:c.324-892A>T
|
ENSP00000407597.1:n.324-892A>T
|
|
ENST00000477087.1:n.285-892A>T
|
|
|
NM_004064.4:c.*9-892A>T
|
NP_004055.1:n.*9-892A>T
|
|
NM_004064.5:c.*9-892A>T
MANE Select
|
NP_004055.1:n.*9-892A>T
|
|