ENST00000703783.1:n.1079A>G
|
|
|
ENST00000703785.1:n.1160A>G
|
|
|
ENST00000262464.9:c.4295A>G
MANE Select
|
ENSP00000262464.4:p.Tyr1432Cys
|
|
ENST00000262464.8:c.4295A>G
|
ENSP00000262464.4:p.Tyr1432Cys
|
|
ENST00000507835.5:c.845A>G
|
ENSP00000426839.1:p.Tyr282Cys
|
|
ENST00000508053.5:c.4295A>G
|
ENSP00000424571.1:p.Tyr1432Cys
|
|
ENST00000508989.5:c.4196A>G
|
ENSP00000425596.1:p.Tyr1399Cys
|
|
ENST00000619499.4:c.4292A>G
|
ENSP00000482132.1:p.Tyr1431Cys
|
|
NM_001999.3:c.4295A>G
|
NP_001990.2:p.Tyr1432Cys
|
|
XM_017009228.2:c.4142A>G
|
XP_016864717.1:p.Tyr1381Cys
|
|
NM_001999.4:c.4295A>G
MANE Select
|
NP_001990.2:p.Tyr1432Cys
|
|