ENST00000700061.1:c.595G>C
|
|
|
ENST00000700062.1:c.595G>C
|
|
|
ENST00000700065.1:n.2511G>C
|
|
|
ENST00000700066.1:c.2015G>C
|
ENSP00000514780.1:p.Arg672Thr
|
|
ENST00000281513.10:c.2498G>C
MANE Select
|
ENSP00000281513.5:p.Arg833Thr
|
|
ENST00000281513.9:c.2498G>C
|
ENSP00000281513.5:p.Arg833Thr
|
|
ENST00000442506.5:c.1G>C
|
|
|
NM_015909.3:c.2498G>C
|
NP_056993.2:p.Arg833Thr
|
|
NR_052013.2:n.2542G>C
|
|
|
XM_011510357.1:c.2369G>C
|
XP_011508659.1:p.Arg790Thr
|
|
XM_011510358.1:c.2498G>C
|
XP_011508660.1:p.Arg833Thr
|
|
XM_011510359.1:c.1859G>C
|
XP_011508661.1:p.Arg620Thr
|
|
XM_011510360.1:c.299G>C
|
XP_011508662.1:p.Arg100Thr
|
|
XM_011510361.1:c.290G>C
|
XP_011508663.1:p.Arg97Thr
|
|
XM_011510357.2:c.2369G>C
|
XP_011508659.1:p.Arg790Thr
|
|
XM_011510358.2:c.2498G>C
|
XP_011508660.1:p.Arg833Thr
|
|
XM_011510360.2:c.299G>C
|
XP_011508662.1:p.Arg100Thr
|
|
XM_011510361.2:c.290G>C
|
XP_011508663.1:p.Arg97Thr
|
|
XM_017004317.1:c.2498G>C
|
XP_016859806.1:p.Arg833Thr
|
|
XM_024452961.1:c.1859G>C
|
XP_024308729.1:p.Arg620Thr
|
|
NM_015909.4:c.2498G>C
MANE Select
|
NP_056993.2:p.Arg833Thr
|
|
NR_052013.3:n.2528G>C
|
|
|