ENST00000696170.1:c.*552A>T
|
ENSP00000512461.1:n.*552A>T
|
|
ENST00000696171.1:c.947A>T
|
ENSP00000512462.1:p.Glu316Val
|
|
ENST00000378588.5:c.1043A>T
MANE Select
|
ENSP00000367851.4:p.Glu348Val
|
|
ENST00000378588.4:c.1043A>T
|
ENSP00000367851.4:p.Glu348Val
|
|
ENST00000465127.1:c.171+378022A>T
|
ENSP00000417050.1:n.171+378022A>T
|
|
ENST00000492288.1:n.468A>T
|
|
|
NM_000397.3:c.1043A>T , LRG_53t1:c.1043A>T
|
NP_000388.2:p.Glu348Val
|
|
XM_011543890.1:c.737A>T
|
XP_011542192.1:p.Glu246Val
|
|
NM_000397.4:c.1043A>T
MANE Select
|
NP_000388.2:p.Glu348Val
|
|