ENST00000328195.8:c.192T>G
MANE Select
|
ENSP00000333551.3:p.Thr64=
|
|
ENST00000328195.7:c.192T>G
|
ENSP00000333551.3:p.Thr64=
|
|
ENST00000518036.5:c.192T>G
|
ENSP00000428005.1:p.Thr64=
|
|
ENST00000520073.5:n.257T>G
|
|
|
ENST00000523187.5:c.36T>G
|
ENSP00000427886.1:p.Thr12=
|
|
ENST00000523358.5:c.192T>G
|
ENSP00000427778.1:p.Thr64=
|
|
ENST00000523994.1:n.197T>G
|
|
|
NM_007198.3:c.192T>G
|
NP_009129.1:p.Thr64=
|
|
NM_001349346.1:c.192T>G
|
NP_001336275.1:p.Thr64=
|
|
NM_001349347.1:c.192T>G
|
NP_001336276.1:p.Thr64=
|
|
NM_001349348.1:c.36T>G
|
NP_001336277.1:p.Thr12=
|
|
NM_001349349.1:c.297T>G
|
NP_001336278.1:p.Thr99=
|
|
NM_007198.4:c.192T>G
MANE Select
|
NP_009129.1:p.Thr64=
|
|
NM_001349346.2:c.192T>G
|
NP_001336275.1:p.Thr64=
|
|
NM_001349347.2:c.192T>G
|
NP_001336276.1:p.Thr64=
|
|
NM_001349348.2:c.36T>G
|
NP_001336277.1:p.Thr12=
|
|