ENST00000703783.1:n.369T>A
|
|
|
ENST00000703785.1:n.450T>A
|
|
|
ENST00000262464.9:c.3585T>A
MANE Select
|
ENSP00000262464.4:p.Arg1195=
|
|
ENST00000262464.8:c.3585T>A
|
ENSP00000262464.4:p.Arg1195=
|
|
ENST00000507835.5:c.135T>A
|
ENSP00000426839.1:p.Arg45=
|
|
ENST00000508053.5:c.3585T>A
|
ENSP00000424571.1:p.Arg1195=
|
|
ENST00000508989.5:c.3486T>A
|
ENSP00000425596.1:p.Arg1162=
|
|
ENST00000619499.4:c.3582T>A
|
ENSP00000482132.1:p.Arg1194=
|
|
NM_001999.3:c.3585T>A
|
NP_001990.2:p.Arg1195=
|
|
XM_017009228.2:c.3432T>A
|
XP_016864717.1:p.Arg1144=
|
|
NM_001999.4:c.3585T>A
MANE Select
|
NP_001990.2:p.Arg1195=
|
|