ENST00000517412.2:n.797G>A
|
|
|
ENST00000517643.2:c.197G>A
|
ENSP00000513333.1:p.Arg66Lys
|
|
ENST00000521657.6:c.197G>A
|
ENSP00000429277.1:p.Arg66Lys
|
|
ENST00000697457.1:c.197G>A
|
ENSP00000513315.1:p.Arg66Lys
|
|
ENST00000697458.1:c.197G>A
|
ENSP00000513316.1:p.Arg66Lys
|
|
ENST00000697459.1:n.414G>A
|
|
|
ENST00000697461.1:c.197G>A
|
ENSP00000513319.1:p.Arg66Lys
|
|
ENST00000697555.1:n.762G>A
|
|
|
ENST00000697556.1:c.197G>A
|
ENSP00000513334.1:p.Arg66Lys
|
|
ENST00000521381.6:c.197G>A
MANE Select
|
ENSP00000428056.1:p.Arg66Lys
|
|
ENST00000517412.1:n.436G>A
|
|
|
ENST00000521381.5:c.197G>A
|
ENSP00000428056.1:p.Arg66Lys
|
|
ENST00000521657.5:c.197G>A
|
ENSP00000429277.1:p.Arg66Lys
|
|
NM_181523.2:c.197G>A
|
NP_852664.1:p.Arg66Lys
|
|
XM_005248542.2:c.197G>A
|
XP_005248599.1:p.Arg66Lys
|
|
XM_005248542.3:c.197G>A
|
XP_005248599.1:p.Arg66Lys
|
|
XM_017009585.2:c.197G>A
|
XP_016865074.1:p.Arg66Lys
|
|
NM_181523.3:c.197G>A
MANE Select
|
NP_852664.1:p.Arg66Lys
|
|