ENST00000696133.1:c.1400+1G>T
|
ENSP00000512426.1:n.1400+1G>T
|
|
ENST00000696134.1:c.*828G>T
|
ENSP00000512427.1:n.*828G>T
|
|
ENST00000367021.8:c.1401G>T
MANE Select
|
ENSP00000355988.3:p.Gln467His
|
|
ENST00000643798.1:c.*911G>T
|
ENSP00000496669.1:n.*911G>T
|
|
ENST00000367021.7:c.1401G>T
|
ENSP00000355988.3:p.Gln467His
|
|
ENST00000542854.5:c.1116G>T
|
ENSP00000440532.1:p.Gln372His
|
|
NM_001206696.1:c.1116G>T
|
NP_001193625.1:p.Gln372His
|
|
NM_006147.3:c.1401G>T
|
NP_006138.1:p.Gln467His
|
|
NM_006147.4:c.1401G>T
MANE Select
|
NP_006138.1:p.Gln467His
|
|
NM_001206696.2:c.1116G>T
|
NP_001193625.1:p.Gln372His
|
|