ENST00000703783.1:n.565G>T
|
|
|
ENST00000703785.1:n.646G>T
|
|
|
ENST00000262464.9:c.3781G>T
MANE Select
|
ENSP00000262464.4:p.Glu1261Ter
|
|
ENST00000262464.8:c.3781G>T
|
ENSP00000262464.4:p.Glu1261Ter
|
|
ENST00000507835.5:c.331G>T
|
ENSP00000426839.1:p.Glu111Ter
|
|
ENST00000508053.5:c.3781G>T
|
ENSP00000424571.1:p.Glu1261Ter
|
|
ENST00000508989.5:c.3682G>T
|
ENSP00000425596.1:p.Glu1228Ter
|
|
ENST00000619499.4:c.3778G>T
|
ENSP00000482132.1:p.Glu1260Ter
|
|
NM_001999.3:c.3781G>T
|
NP_001990.2:p.Glu1261Ter
|
|
XM_017009228.2:c.3628G>T
|
XP_016864717.1:p.Glu1210Ter
|
|
NM_001999.4:c.3781G>T
MANE Select
|
NP_001990.2:p.Glu1261Ter
|
|