ENST00000703783.1:n.336C>T
|
|
|
ENST00000703785.1:n.417C>T
|
|
|
ENST00000262464.9:c.3552C>T
MANE Select
|
ENSP00000262464.4:p.Asp1184=
|
|
ENST00000262464.8:c.3552C>T
|
ENSP00000262464.4:p.Asp1184=
|
|
ENST00000507835.5:c.102C>T
|
ENSP00000426839.1:p.Asp34=
|
|
ENST00000508053.5:c.3552C>T
|
ENSP00000424571.1:p.Asp1184=
|
|
ENST00000508989.5:c.3453C>T
|
ENSP00000425596.1:p.Asp1151=
|
|
ENST00000619499.4:c.3549C>T
|
ENSP00000482132.1:p.Asp1183=
|
|
NM_001999.3:c.3552C>T
|
NP_001990.2:p.Asp1184=
|
|
XM_017009228.2:c.3399C>T
|
XP_016864717.1:p.Asp1133=
|
|
NM_001999.4:c.3552C>T
MANE Select
|
NP_001990.2:p.Asp1184=
|
|