ENST00000700061.1:c.4388C>T
|
|
|
ENST00000700062.1:c.4426+13619C>T
|
|
|
ENST00000700063.1:c.913C>T
|
|
|
ENST00000700064.1:c.2258C>T
|
|
|
ENST00000281513.10:c.6402C>T
MANE Select
|
ENSP00000281513.5:p.Ala2134=
|
|
ENST00000281513.9:c.6402C>T
|
ENSP00000281513.5:p.Ala2134=
|
|
ENST00000417461.5:c.512+13619C>T
|
ENSP00000392421.1:n.512+13619C>T
|
|
ENST00000442506.5:c.3545C>T
|
|
|
NM_015909.3:c.6402C>T
|
NP_056993.2:p.Ala2134=
|
|
NR_052013.2:n.6280+13619C>T
|
|
|
XM_011510357.1:c.6273C>T
|
XP_011508659.1:p.Ala2091=
|
|
XM_011510358.1:c.6402C>T
|
XP_011508660.1:p.Ala2134=
|
|
XM_011510359.1:c.5763C>T
|
XP_011508661.1:p.Ala1921=
|
|
XM_011510360.1:c.4203C>T
|
XP_011508662.1:p.Ala1401=
|
|
XM_011510361.1:c.4194C>T
|
XP_011508663.1:p.Ala1398=
|
|
XM_011510357.2:c.6273C>T
|
XP_011508659.1:p.Ala2091=
|
|
XM_011510358.2:c.6402C>T
|
XP_011508660.1:p.Ala2134=
|
|
XM_011510360.2:c.4203C>T
|
XP_011508662.1:p.Ala1401=
|
|
XM_011510361.2:c.4194C>T
|
XP_011508663.1:p.Ala1398=
|
|
XM_017004317.1:c.6402C>T
|
XP_016859806.1:p.Ala2134=
|
|
XM_024452961.1:c.5763C>T
|
XP_024308729.1:p.Ala1921=
|
|
NM_015909.4:c.6402C>T
MANE Select
|
NP_056993.2:p.Ala2134=
|
|
NR_052013.3:n.6266+13619C>T
|
|
|