ENST00000283871.10:c.930G>C
MANE Select
|
ENSP00000283871.5:p.Val310=
|
|
ENST00000283871.9:c.930G>C
|
ENSP00000283871.5:p.Val310=
|
|
ENST00000470321.1:n.270G>C
|
|
|
ENST00000475447.2:c.307+3058G>C
|
|
|
ENST00000492108.5:c.285+3058G>C
|
ENSP00000419838.1:n.285+3058G>C
|
|
ENST00000494453.1:c.350G>C
|
|
|
NM_000187.3:c.930G>C
|
NP_000178.2:p.Val310=
|
|
XM_005247412.1:c.705G>C
|
XP_005247469.1:p.Val235=
|
|
XM_005247413.1:c.930G>C
|
XP_005247470.1:p.Val310=
|
|
XM_011512746.1:c.879+3058G>C
|
XP_011511048.1:n.879+3058G>C
|
|
XM_005247412.2:c.705G>C
|
XP_005247469.1:p.Val235=
|
|
XM_005247413.2:c.930G>C
|
XP_005247470.1:p.Val310=
|
|
XM_011512746.2:c.879+3058G>C
|
XP_011511048.1:n.879+3058G>C
|
|
XM_017006277.2:c.507G>C
|
XP_016861766.1:p.Val169=
|
|
NM_000187.4:c.930G>C
MANE Select
|
NP_000178.2:p.Val310=
|
|