ENST00000703783.1:n.571A>T
|
|
|
ENST00000703785.1:n.652A>T
|
|
|
ENST00000262464.9:c.3787A>T
MANE Select
|
ENSP00000262464.4:p.Ser1263Cys
|
|
ENST00000262464.8:c.3787A>T
|
ENSP00000262464.4:p.Ser1263Cys
|
|
ENST00000507835.5:c.337A>T
|
ENSP00000426839.1:p.Ser113Cys
|
|
ENST00000508053.5:c.3787A>T
|
ENSP00000424571.1:p.Ser1263Cys
|
|
ENST00000508989.5:c.3688A>T
|
ENSP00000425596.1:p.Ser1230Cys
|
|
ENST00000619499.4:c.3784A>T
|
ENSP00000482132.1:p.Ser1262Cys
|
|
NM_001999.3:c.3787A>T
|
NP_001990.2:p.Ser1263Cys
|
|
XM_017009228.2:c.3634A>T
|
XP_016864717.1:p.Ser1212Cys
|
|
NM_001999.4:c.3787A>T
MANE Select
|
NP_001990.2:p.Ser1263Cys
|
|