ENST00000703783.1:n.270T>A
|
|
|
ENST00000703785.1:n.351T>A
|
|
|
ENST00000262464.9:c.3486T>A
MANE Select
|
ENSP00000262464.4:p.Cys1162Ter
|
|
ENST00000262464.8:c.3486T>A
|
ENSP00000262464.4:p.Cys1162Ter
|
|
ENST00000507835.5:c.36T>A
|
ENSP00000426839.1:p.Cys12Ter
|
|
ENST00000508053.5:c.3486T>A
|
ENSP00000424571.1:p.Cys1162Ter
|
|
ENST00000508989.5:c.3387T>A
|
ENSP00000425596.1:p.Cys1129Ter
|
|
ENST00000619499.4:c.3483T>A
|
ENSP00000482132.1:p.Cys1161Ter
|
|
NM_001999.3:c.3486T>A
|
NP_001990.2:p.Cys1162Ter
|
|
XM_017009228.2:c.3333T>A
|
XP_016864717.1:p.Cys1111Ter
|
|
NM_001999.4:c.3486T>A
MANE Select
|
NP_001990.2:p.Cys1162Ter
|
|