ENST00000700061.1:c.674+238T=
|
|
|
ENST00000700062.1:c.674+238T=
|
|
|
ENST00000700065.1:n.2590+238T=
|
|
|
ENST00000700066.1:c.2094+238T=
|
ENSP00000514780.1:n.2094+238T=
|
|
ENST00000281513.10:c.2577+238T=
MANE Select
|
ENSP00000281513.5:n.2577+238T=
|
|
ENST00000281513.9:c.2577+238T=
|
ENSP00000281513.5:n.2577+238T=
|
|
ENST00000441755.5:c.78+238T=
|
ENSP00000396501.1:n.78+238T=
|
|
ENST00000442506.5:c.80+238T=
|
|
|
NM_015909.3:c.2577+238T=
|
NP_056993.2:n.2577+238T=
|
|
NR_052013.2:n.2621+238T=
|
|
|
XM_011510357.1:c.2448+238T=
|
XP_011508659.1:n.2448+238T=
|
|
XM_011510358.1:c.2577+238T=
|
XP_011508660.1:n.2577+238T=
|
|
XM_011510359.1:c.1938+238T=
|
XP_011508661.1:n.1938+238T=
|
|
XM_011510360.1:c.378+238T=
|
XP_011508662.1:n.378+238T=
|
|
XM_011510361.1:c.369+238T=
|
XP_011508663.1:n.369+238T=
|
|
XM_011510357.2:c.2448+238T=
|
XP_011508659.1:n.2448+238T=
|
|
XM_011510358.2:c.2577+238T=
|
XP_011508660.1:n.2577+238T=
|
|
XM_011510360.2:c.378+238T=
|
XP_011508662.1:n.378+238T=
|
|
XM_011510361.2:c.369+238T=
|
XP_011508663.1:n.369+238T=
|
|
XM_017004317.1:c.2577+238T=
|
XP_016859806.1:n.2577+238T=
|
|
XM_024452961.1:c.1938+238T=
|
XP_024308729.1:n.1938+238T=
|
|
NM_015909.4:c.2577+238T=
MANE Select
|
NP_056993.2:n.2577+238T=
|
|
NR_052013.3:n.2607+238T=
|
|
|