ENST00000703783.1:n.360A>T
|
|
|
ENST00000703785.1:n.441A>T
|
|
|
ENST00000262464.9:c.3576A>T
MANE Select
|
ENSP00000262464.4:p.Ser1192=
|
|
ENST00000262464.8:c.3576A>T
|
ENSP00000262464.4:p.Ser1192=
|
|
ENST00000507835.5:c.126A>T
|
ENSP00000426839.1:p.Ser42=
|
|
ENST00000508053.5:c.3576A>T
|
ENSP00000424571.1:p.Ser1192=
|
|
ENST00000508989.5:c.3477A>T
|
ENSP00000425596.1:p.Ser1159=
|
|
ENST00000619499.4:c.3573A>T
|
ENSP00000482132.1:p.Ser1191=
|
|
NM_001999.3:c.3576A>T
|
NP_001990.2:p.Ser1192=
|
|
XM_017009228.2:c.3423A>T
|
XP_016864717.1:p.Ser1141=
|
|
NM_001999.4:c.3576A>T
MANE Select
|
NP_001990.2:p.Ser1192=
|
|