ENST00000394867.9:n.1545T>C
|
|
|
ENST00000688002.1:n.3257T>C
|
|
|
ENST00000688751.1:n.242T>C
|
|
|
ENST00000689792.1:n.1010T>C
|
|
|
ENST00000262948.10:c.1106T>C
MANE Select
|
ENSP00000262948.4:p.Ile369Thr
|
|
ENST00000262948.9:c.1106T>C
|
ENSP00000262948.3:p.Ile369Thr
|
|
ENST00000394867.8:c.815T>C
|
ENSP00000378336.1:p.Ile272Thr
|
|
ENST00000597263.5:n.291T>C
|
|
|
ENST00000599021.1:c.216T>C
|
|
|
ENST00000600584.5:n.2555T>C
|
|
|
ENST00000601786.5:n.1407T>C
|
|
|
NM_030662.3:c.1106T>C , LRG_750t1:c.1106T>C
|
NP_109587.1:p.Ile369Thr
|
|
XM_006722799.2:c.827T>C
|
XP_006722862.1:p.Ile276Thr
|
|
XM_011528133.1:c.536T>C
|
XP_011526435.1:p.Ile179Thr
|
|
NM_030662.4:c.1106T>C
MANE Select
|
NP_109587.1:p.Ile369Thr
|
|