ENST00000703783.1:n.587G>A
|
|
|
ENST00000703785.1:n.668G>A
|
|
|
ENST00000262464.9:c.3803G>A
MANE Select
|
ENSP00000262464.4:p.Cys1268Tyr
|
|
ENST00000262464.8:c.3803G>A
|
ENSP00000262464.4:p.Cys1268Tyr
|
|
ENST00000507835.5:c.353G>A
|
ENSP00000426839.1:p.Cys118Tyr
|
|
ENST00000508053.5:c.3803G>A
|
ENSP00000424571.1:p.Cys1268Tyr
|
|
ENST00000508989.5:c.3704G>A
|
ENSP00000425596.1:p.Cys1235Tyr
|
|
ENST00000619499.4:c.3800G>A
|
ENSP00000482132.1:p.Cys1267Tyr
|
|
NM_001999.3:c.3803G>A
|
NP_001990.2:p.Cys1268Tyr
|
|
XM_017009228.2:c.3650G>A
|
XP_016864717.1:p.Cys1217Tyr
|
|
NM_001999.4:c.3803G>A
MANE Select
|
NP_001990.2:p.Cys1268Tyr
|
|