ENST00000703783.1:n.1080C>A
|
|
|
ENST00000703785.1:n.1161C>A
|
|
|
ENST00000262464.9:c.4296C>A
MANE Select
|
ENSP00000262464.4:p.Tyr1432Ter
|
|
ENST00000262464.8:c.4296C>A
|
ENSP00000262464.4:p.Tyr1432Ter
|
|
ENST00000507835.5:c.846C>A
|
ENSP00000426839.1:p.Tyr282Ter
|
|
ENST00000508053.5:c.4296C>A
|
ENSP00000424571.1:p.Tyr1432Ter
|
|
ENST00000508989.5:c.4197C>A
|
ENSP00000425596.1:p.Tyr1399Ter
|
|
ENST00000619499.4:c.4293C>A
|
ENSP00000482132.1:p.Tyr1431Ter
|
|
NM_001999.3:c.4296C>A
|
NP_001990.2:p.Tyr1432Ter
|
|
XM_017009228.2:c.4143C>A
|
XP_016864717.1:p.Tyr1381Ter
|
|
NM_001999.4:c.4296C>A
MANE Select
|
NP_001990.2:p.Tyr1432Ter
|
|