ENST00000696170.1:c.*44G>T
|
ENSP00000512461.1:n.*44G>T
|
|
ENST00000696171.1:c.439G>T
|
ENSP00000512462.1:p.Gly147Ter
|
|
ENST00000696172.1:c.338-2953G>T
|
ENSP00000512463.1:n.338-2953G>T
|
|
ENST00000378588.5:c.535G>T
MANE Select
|
ENSP00000367851.4:p.Gly179Ter
|
|
ENST00000378588.4:c.535G>T
|
ENSP00000367851.4:p.Gly179Ter
|
|
ENST00000465127.1:c.171+370002G>T
|
ENSP00000417050.1:n.171+370002G>T
|
|
NM_000397.3:c.535G>T , LRG_53t1:c.535G>T
|
NP_000388.2:p.Gly179Ter
|
|
XM_011543890.1:c.229G>T
|
XP_011542192.1:p.Gly77Ter
|
|
NM_000397.4:c.535G>T
MANE Select
|
NP_000388.2:p.Gly179Ter
|
|