ENST00000703783.1:n.591T>C
|
|
|
ENST00000703785.1:n.672T>C
|
|
|
ENST00000262464.9:c.3807T>C
MANE Select
|
ENSP00000262464.4:p.Ser1269=
|
|
ENST00000262464.8:c.3807T>C
|
ENSP00000262464.4:p.Ser1269=
|
|
ENST00000507835.5:c.357T>C
|
ENSP00000426839.1:p.Ser119=
|
|
ENST00000508053.5:c.3807T>C
|
ENSP00000424571.1:p.Ser1269=
|
|
ENST00000508989.5:c.3708T>C
|
ENSP00000425596.1:p.Ser1236=
|
|
ENST00000619499.4:c.3804T>C
|
ENSP00000482132.1:p.Ser1268=
|
|
NM_001999.3:c.3807T>C
|
NP_001990.2:p.Ser1269=
|
|
XM_017009228.2:c.3654T>C
|
XP_016864717.1:p.Ser1218=
|
|
NM_001999.4:c.3807T>C
MANE Select
|
NP_001990.2:p.Ser1269=
|
|