ENST00000539111.7:c.428G>C
MANE Select
|
ENSP00000442563.2:p.Ser143Thr
|
|
ENST00000585104.2:n.399G>C
|
|
|
ENST00000671755.1:c.399G>C
|
|
|
ENST00000673460.1:c.399G>C
|
|
|
ENST00000539111.6:c.428G>C
|
ENSP00000442563.2:p.Ser143Thr
|
|
ENST00000578997.1:c.215G>C
|
ENSP00000464389.1:p.Ser72Thr
|
|
ENST00000585141.5:n.479G>C
|
|
|
NM_007215.3:c.428G>C
|
NP_009146.2:p.Ser143Thr
|
|
XM_006721651.2:c.428G>C
|
XP_006721714.1:p.Ser143Thr
|
|
XR_243630.1:n.479G>C
|
|
|
XR_934357.1:n.479G>C
|
|
|
XR_934358.1:n.479G>C
|
|
|
NM_007215.4:c.428G>C
MANE Select
|
NP_009146.2:p.Ser143Thr
|
|