ENST00000703783.1:n.620G>T
|
|
|
ENST00000703785.1:n.701G>T
|
|
|
ENST00000262464.9:c.3836G>T
MANE Select
|
ENSP00000262464.4:p.Arg1279Ile
|
|
ENST00000262464.8:c.3836G>T
|
ENSP00000262464.4:p.Arg1279Ile
|
|
ENST00000507835.5:c.386G>T
|
ENSP00000426839.1:p.Arg129Ile
|
|
ENST00000508053.5:c.3836G>T
|
ENSP00000424571.1:p.Arg1279Ile
|
|
ENST00000508989.5:c.3737G>T
|
ENSP00000425596.1:p.Arg1246Ile
|
|
ENST00000619499.4:c.3833G>T
|
ENSP00000482132.1:p.Arg1278Ile
|
|
NM_001999.3:c.3836G>T
|
NP_001990.2:p.Arg1279Ile
|
|
XM_017009228.2:c.3683G>T
|
XP_016864717.1:p.Arg1228Ile
|
|
NM_001999.4:c.3836G>T
MANE Select
|
NP_001990.2:p.Arg1279Ile
|
|