ENST00000283871.10:c.427G>T
MANE Select
|
ENSP00000283871.5:p.Glu143Ter
|
|
ENST00000283871.9:c.427G>T
|
ENSP00000283871.5:p.Glu143Ter
|
|
ENST00000476082.2:c.304G>T
|
ENSP00000419560.2:p.Glu102Ter
|
|
ENST00000492108.5:c.58G>T
|
ENSP00000419838.1:p.Glu20Ter
|
|
NM_000187.3:c.427G>T
|
NP_000178.2:p.Glu143Ter
|
|
XM_005247412.1:c.427G>T
|
XP_005247469.1:p.Glu143Ter
|
|
XM_005247413.1:c.427G>T
|
XP_005247470.1:p.Glu143Ter
|
|
XM_005247414.3:c.427G>T
|
XP_005247471.1:p.Glu143Ter
|
|
XM_011512746.1:c.427G>T
|
XP_011511048.1:p.Glu143Ter
|
|
XM_005247412.2:c.427G>T
|
XP_005247469.1:p.Glu143Ter
|
|
XM_005247413.2:c.427G>T
|
XP_005247470.1:p.Glu143Ter
|
|
XM_005247414.5:c.427G>T
|
XP_005247471.1:p.Glu143Ter
|
|
XM_011512746.2:c.427G>T
|
XP_011511048.1:p.Glu143Ter
|
|
XM_017006277.2:c.4G>T
|
XP_016861766.1:p.Glu2Ter
|
|
NM_000187.4:c.427G>T
MANE Select
|
NP_000178.2:p.Glu143Ter
|
|