ENST00000394867.9:n.1497A>C
|
|
|
ENST00000688002.1:n.3209A>C
|
|
|
ENST00000688751.1:n.194A>C
|
|
|
ENST00000689792.1:n.962A>C
|
|
|
ENST00000262948.10:c.1058A>C
MANE Select
|
ENSP00000262948.4:p.Asn353Thr
|
|
ENST00000262948.9:c.1058A>C
|
ENSP00000262948.3:p.Asn353Thr
|
|
ENST00000394867.8:c.767A>C
|
ENSP00000378336.1:p.Asn256Thr
|
|
ENST00000597263.5:n.243A>C
|
|
|
ENST00000599021.1:c.168A>C
|
|
|
ENST00000600584.5:n.2507A>C
|
|
|
ENST00000601786.5:n.1359A>C
|
|
|
NM_030662.3:c.1058A>C , LRG_750t1:c.1058A>C
|
NP_109587.1:p.Asn353Thr
|
|
XM_006722799.2:c.779A>C
|
XP_006722862.1:p.Asn260Thr
|
|
XM_011528133.1:c.488A>C
|
XP_011526435.1:p.Asn163Thr
|
|
NM_030662.4:c.1058A>C
MANE Select
|
NP_109587.1:p.Asn353Thr
|
|