ENST00000700061.1:c.645G>T
|
|
|
ENST00000700062.1:c.645G>T
|
|
|
ENST00000700065.1:n.2561G>T
|
|
|
ENST00000700066.1:c.2065G>T
|
ENSP00000514780.1:p.Ala689Ser
|
|
ENST00000281513.10:c.2548G>T
MANE Select
|
ENSP00000281513.5:p.Ala850Ser
|
|
ENST00000281513.9:c.2548G>T
|
ENSP00000281513.5:p.Ala850Ser
|
|
ENST00000441755.5:c.49G>T
|
ENSP00000396501.1:p.Ala17Ser
|
|
ENST00000442506.5:c.51G>T
|
|
|
NM_015909.3:c.2548G>T
|
NP_056993.2:p.Ala850Ser
|
|
NR_052013.2:n.2592G>T
|
|
|
XM_011510357.1:c.2419G>T
|
XP_011508659.1:p.Ala807Ser
|
|
XM_011510358.1:c.2548G>T
|
XP_011508660.1:p.Ala850Ser
|
|
XM_011510359.1:c.1909G>T
|
XP_011508661.1:p.Ala637Ser
|
|
XM_011510360.1:c.349G>T
|
XP_011508662.1:p.Ala117Ser
|
|
XM_011510361.1:c.340G>T
|
XP_011508663.1:p.Ala114Ser
|
|
XM_011510357.2:c.2419G>T
|
XP_011508659.1:p.Ala807Ser
|
|
XM_011510358.2:c.2548G>T
|
XP_011508660.1:p.Ala850Ser
|
|
XM_011510360.2:c.349G>T
|
XP_011508662.1:p.Ala117Ser
|
|
XM_011510361.2:c.340G>T
|
XP_011508663.1:p.Ala114Ser
|
|
XM_017004317.1:c.2548G>T
|
XP_016859806.1:p.Ala850Ser
|
|
XM_024452961.1:c.1909G>T
|
XP_024308729.1:p.Ala637Ser
|
|
NM_015909.4:c.2548G>T
MANE Select
|
NP_056993.2:p.Ala850Ser
|
|
NR_052013.3:n.2578G>T
|
|
|