ENST00000696133.1:c.1400+2293G>T
|
ENSP00000512426.1:n.1400+2293G>T
|
|
ENST00000696134.1:c.*3120G>T
|
ENSP00000512427.1:n.*3120G>T
|
|
ENST00000367021.8:c.*2289G>T
MANE Select
|
ENSP00000355988.3:n.*2289G>T
|
|
ENST00000367021.7:c.*2289G>T
|
ENSP00000355988.3:n.*2289G>T
|
|
ENST00000542854.5:c.*2289G>T
|
ENSP00000440532.1:n.*2289G>T
|
|
NM_001206696.1:c.*2289G>T
|
NP_001193625.1:n.*2289G>T
|
|
NM_006147.3:c.*2289G>T
|
NP_006138.1:n.*2289G>T
|
|
NM_006147.4:c.*2289G>T
MANE Select
|
NP_006138.1:n.*2289G>T
|
|
NM_001206696.2:c.*2289G>T
|
NP_001193625.1:n.*2289G>T
|
|