ENST00000394867.9:n.1620C>T
|
|
|
ENST00000688002.1:n.3332C>T
|
|
|
ENST00000688751.1:n.317C>T
|
|
|
ENST00000689792.1:n.1085C>T
|
|
|
ENST00000262948.10:c.1181C>T
MANE Select
|
ENSP00000262948.4:p.Thr394Ile
|
|
ENST00000262948.9:c.1181C>T
|
ENSP00000262948.3:p.Thr394Ile
|
|
ENST00000394867.8:c.890C>T
|
ENSP00000378336.1:p.Thr297Ile
|
|
ENST00000597263.5:n.366C>T
|
|
|
ENST00000599021.1:c.291C>T
|
|
|
ENST00000600584.5:n.2630C>T
|
|
|
ENST00000601786.5:n.1482C>T
|
|
|
NM_030662.3:c.1181C>T , LRG_750t1:c.1181C>T
|
NP_109587.1:p.Thr394Ile
|
|
XM_006722799.2:c.902C>T
|
XP_006722862.1:p.Thr301Ile
|
|
XM_011528133.1:c.611C>T
|
XP_011526435.1:p.Thr204Ile
|
|
NM_030662.4:c.1181C>T
MANE Select
|
NP_109587.1:p.Thr394Ile
|
|