ENST00000696133.1:c.1312C>T
|
ENSP00000512426.1:p.Gln438Ter
|
|
ENST00000696134.1:c.*739C>T
|
ENSP00000512427.1:n.*739C>T
|
|
ENST00000367021.8:c.1312C>T
MANE Select
|
ENSP00000355988.3:p.Gln438Ter
|
|
ENST00000643798.1:c.*822C>T
|
ENSP00000496669.1:n.*822C>T
|
|
ENST00000367021.7:c.1312C>T
|
ENSP00000355988.3:p.Gln438Ter
|
|
ENST00000542854.5:c.1027C>T
|
ENSP00000440532.1:p.Gln343Ter
|
|
NM_001206696.1:c.1027C>T
|
NP_001193625.1:p.Gln343Ter
|
|
NM_006147.3:c.1312C>T
|
NP_006138.1:p.Gln438Ter
|
|
NM_006147.4:c.1312C>T
MANE Select
|
NP_006138.1:p.Gln438Ter
|
|
NM_001206696.2:c.1027C>T
|
NP_001193625.1:p.Gln343Ter
|
|