ENST00000322344.8:c.1187G>C
MANE Select
|
ENSP00000323511.2:p.Arg396Thr
|
|
ENST00000322344.7:c.1187G>C
|
ENSP00000323511.2:p.Arg396Thr
|
|
ENST00000593706.3:n.621G>C
|
|
|
ENST00000593946.5:c.*1114G>C
|
ENSP00000468896.1:n.*1114G>C
|
|
ENST00000594661.5:n.1688G>C
|
|
|
ENST00000596014.5:c.1187G>C
|
ENSP00000472300.1:p.Arg396Thr
|
|
ENST00000599454.5:n.31G>C
|
|
|
ENST00000600573.5:c.1094G>C
|
ENSP00000469826.1:p.Arg365Thr
|
|
ENST00000600910.5:c.1187G>C
|
ENSP00000473137.1:p.Arg396Thr
|
|
ENST00000601816.3:n.86G>C
|
|
|
ENST00000625216.2:c.268G>C
|
ENSP00000486898.1:n.268G>C
|
|
ENST00000627232.2:c.1107G>C
|
ENSP00000486037.1:n.1107G>C
|
|
ENST00000631020.2:c.1079G>C
|
ENSP00000486707.1:p.Arg360Thr
|
|
NM_007254.3:c.1187G>C
|
NP_009185.2:p.Arg396Thr
|
|
NM_007254.4:c.1187G>C
MANE Select
|
NP_009185.2:p.Arg396Thr
|
|