ENST00000700061.1:c.615G>T
|
|
|
ENST00000700062.1:c.615G>T
|
|
|
ENST00000700065.1:n.2531G>T
|
|
|
ENST00000700066.1:c.2035G>T
|
ENSP00000514780.1:p.Glu679Ter
|
|
ENST00000281513.10:c.2518G>T
MANE Select
|
ENSP00000281513.5:p.Glu840Ter
|
|
ENST00000281513.9:c.2518G>T
|
ENSP00000281513.5:p.Glu840Ter
|
|
ENST00000441755.5:c.19G>T
|
ENSP00000396501.1:p.Glu7Ter
|
|
ENST00000442506.5:c.21G>T
|
|
|
NM_015909.3:c.2518G>T
|
NP_056993.2:p.Glu840Ter
|
|
NR_052013.2:n.2562G>T
|
|
|
XM_011510357.1:c.2389G>T
|
XP_011508659.1:p.Glu797Ter
|
|
XM_011510358.1:c.2518G>T
|
XP_011508660.1:p.Glu840Ter
|
|
XM_011510359.1:c.1879G>T
|
XP_011508661.1:p.Glu627Ter
|
|
XM_011510360.1:c.319G>T
|
XP_011508662.1:p.Glu107Ter
|
|
XM_011510361.1:c.310G>T
|
XP_011508663.1:p.Glu104Ter
|
|
XM_011510357.2:c.2389G>T
|
XP_011508659.1:p.Glu797Ter
|
|
XM_011510358.2:c.2518G>T
|
XP_011508660.1:p.Glu840Ter
|
|
XM_011510360.2:c.319G>T
|
XP_011508662.1:p.Glu107Ter
|
|
XM_011510361.2:c.310G>T
|
XP_011508663.1:p.Glu104Ter
|
|
XM_017004317.1:c.2518G>T
|
XP_016859806.1:p.Glu840Ter
|
|
XM_024452961.1:c.1879G>T
|
XP_024308729.1:p.Glu627Ter
|
|
NM_015909.4:c.2518G>T
MANE Select
|
NP_056993.2:p.Glu840Ter
|
|
NR_052013.3:n.2548G>T
|
|
|