ENST00000558767.6:c.399T>G
|
ENSP00000507680.1:p.His133Gln
|
|
ENST00000682012.1:n.474T>G
|
|
|
ENST00000683593.1:n.2062T>G
|
|
|
ENST00000684363.1:c.365-112T>G
|
ENSP00000507314.1:n.365-112T>G
|
|
ENST00000684569.1:n.444T>G
|
|
|
ENST00000561421.6:c.399T>G
MANE Select
|
ENSP00000453347.2:p.His133Gln
|
|
ENST00000646551.1:n.1886T>G
|
|
|
ENST00000261755.9:c.399T>G
|
ENSP00000261755.5:p.His133Gln
|
|
ENST00000407106.5:c.399T>G
|
ENSP00000385080.1:p.His133Gln
|
|
ENST00000537726.5:n.545T>G
|
|
|
ENST00000539156.5:c.189T>G
|
ENSP00000454271.1:p.His63Gln
|
|
ENST00000558022.5:c.399T>G
|
ENSP00000453152.1:p.His133Gln
|
|
ENST00000558627.1:n.327T>G
|
|
|
ENST00000558767.5:n.660T>G
|
|
|
ENST00000561369.1:n.543T>G
|
|
|
ENST00000561421.5:c.399T>G
|
ENSP00000453347.1:p.His133Gln
|
|
NM_000137.2:c.399T>G
|
NP_000128.1:p.His133Gln
|
|
XM_024449872.1:c.399T>G
|
XP_024305640.1:p.His133Gln
|
|
NM_000137.4:c.399T>G
MANE Select
|
NP_000128.1:p.His133Gln
|
|
NM_001374377.1:c.399T>G
|
NP_001361306.1:p.His133Gln
|
|
NM_001374380.1:c.399T>G
|
NP_001361309.1:p.His133Gln
|
|