ENST00000281928.9:c.5588G>C
MANE Select
|
ENSP00000281928.3:p.Arg1863Thr
|
|
ENST00000548694.2:n.377G>C
|
|
|
ENST00000648379.1:n.3956G>C
|
|
|
ENST00000648737.1:n.5352G>C
|
|
|
ENST00000648825.1:n.3773G>C
|
|
|
ENST00000648916.1:n.3599G>C
|
|
|
ENST00000649607.1:c.3772G>C
|
|
|
ENST00000649775.1:c.2077G>C
|
|
|
ENST00000650226.1:c.5588G>C
|
ENSP00000496981.1:p.Arg1863Thr
|
|
ENST00000281928.7:c.5588G>C
|
ENSP00000281928.3:p.Arg1863Thr
|
|
ENST00000548694.1:n.377G>C
|
|
|
ENST00000552447.1:c.165G>C
|
|
|
NM_015335.4:c.5588G>C
|
NP_056150.1:p.Arg1863Thr
|
|
XM_011538080.1:c.5588G>C
|
XP_011536382.1:p.Arg1863Thr
|
|
XM_011538081.1:c.5585G>C
|
XP_011536383.1:p.Arg1862Thr
|
|
XM_011538082.1:c.5558G>C
|
XP_011536384.1:p.Arg1853Thr
|
|
XM_011538080.2:c.5588G>C
|
XP_011536382.1:p.Arg1863Thr
|
|
XM_011538081.2:c.5585G>C
|
XP_011536383.1:p.Arg1862Thr
|
|
XM_011538082.2:c.5558G>C
|
XP_011536384.1:p.Arg1853Thr
|
|
XM_017019090.1:c.5585G>C
|
XP_016874579.1:p.Arg1862Thr
|
|
NM_015335.5:c.5588G>C
MANE Select
|
NP_056150.1:p.Arg1863Thr
|
|