ENST00000394867.9:n.1624C>T
|
|
|
ENST00000688002.1:n.3336C>T
|
|
|
ENST00000688751.1:n.321C>T
|
|
|
ENST00000689792.1:n.1089C>T
|
|
|
ENST00000262948.10:c.1185C>T
MANE Select
|
ENSP00000262948.4:p.Pro395=
|
|
ENST00000262948.9:c.1185C>T
|
ENSP00000262948.3:p.Pro395=
|
|
ENST00000394867.8:c.894C>T
|
ENSP00000378336.1:p.Pro298=
|
|
ENST00000597263.5:n.370C>T
|
|
|
ENST00000599021.1:c.295C>T
|
|
|
ENST00000600584.5:n.2634C>T
|
|
|
ENST00000601786.5:n.1486C>T
|
|
|
NM_030662.3:c.1185C>T , LRG_750t1:c.1185C>T
|
NP_109587.1:p.Pro395=
|
|
XM_006722799.2:c.906C>T
|
XP_006722862.1:p.Pro302=
|
|
XM_011528133.1:c.615C>T
|
XP_011526435.1:p.Pro205=
|
|
NM_030662.4:c.1185C>T
MANE Select
|
NP_109587.1:p.Pro395=
|
|