ENST00000703783.1:n.1008T>C
|
|
|
ENST00000703785.1:n.1089T>C
|
|
|
ENST00000262464.9:c.4224T>C
MANE Select
|
ENSP00000262464.4:p.Asp1408=
|
|
ENST00000262464.8:c.4224T>C
|
ENSP00000262464.4:p.Asp1408=
|
|
ENST00000507835.5:c.774T>C
|
ENSP00000426839.1:p.Asp258=
|
|
ENST00000508053.5:c.4224T>C
|
ENSP00000424571.1:p.Asp1408=
|
|
ENST00000508989.5:c.4125T>C
|
ENSP00000425596.1:p.Asp1375=
|
|
ENST00000619499.4:c.4221T>C
|
ENSP00000482132.1:p.Asp1407=
|
|
NM_001999.3:c.4224T>C
|
NP_001990.2:p.Asp1408=
|
|
XM_017009228.2:c.4071T>C
|
XP_016864717.1:p.Asp1357=
|
|
NM_001999.4:c.4224T>C
MANE Select
|
NP_001990.2:p.Asp1408=
|
|