ENST00000612619.2:c.117G>A
|
ENSP00000479970.1:p.Arg39=
|
|
ENST00000694948.1:n.215G>A
|
|
|
ENST00000694949.1:n.212G>A
|
|
|
ENST00000694950.1:c.197G>A
|
|
|
ENST00000319363.11:c.117G>A
MANE Select
|
ENSP00000320936.6:p.Arg39=
|
|
ENST00000319363.10:c.117G>A
|
ENSP00000320936.6:p.Arg39=
|
|
ENST00000459971.1:n.152G>A
|
|
|
ENST00000477874.1:n.255G>A
|
|
|
ENST00000612619.1:c.117G>A
|
ENSP00000479970.1:p.Arg39=
|
|
NM_001289905.1:c.117G>A
|
NP_001276834.1:p.Arg39=
|
|
NM_014339.6:c.117G>A , LRG_355t1:c.117G>A
|
NP_055154.3:p.Arg39=
|
|
NM_014339.7:c.117G>A
MANE Select
|
NP_055154.3:p.Arg39=
|
|
NM_001289905.2:c.117G>A
|
NP_001276834.1:p.Arg39=
|
|