ENST00000703783.1:n.1092C>A
|
|
|
ENST00000703785.1:n.1173C>A
|
|
|
ENST00000262464.9:c.4308C>A
MANE Select
|
ENSP00000262464.4:p.Cys1436Ter
|
|
ENST00000262464.8:c.4308C>A
|
ENSP00000262464.4:p.Cys1436Ter
|
|
ENST00000507835.5:c.858C>A
|
ENSP00000426839.1:p.Cys286Ter
|
|
ENST00000508053.5:c.4308C>A
|
ENSP00000424571.1:p.Cys1436Ter
|
|
ENST00000508989.5:c.4209C>A
|
ENSP00000425596.1:p.Cys1403Ter
|
|
ENST00000619499.4:c.4305C>A
|
ENSP00000482132.1:p.Cys1435Ter
|
|
NM_001999.3:c.4308C>A
|
NP_001990.2:p.Cys1436Ter
|
|
XM_017009228.2:c.4155C>A
|
XP_016864717.1:p.Cys1385Ter
|
|
NM_001999.4:c.4308C>A
MANE Select
|
NP_001990.2:p.Cys1436Ter
|
|