|
NM_181523.3:c.484C>T
MANE Select
|
NP_852664.1:p.Arg162Ter
|
|
ENST00000521381.6:c.484C>T
MANE Select
|
ENSP00000428056.1:p.Arg162Ter
|
|
NM_181523.2:c.484C>T
|
NP_852664.1:p.Arg162Ter
|
|
ENST00000517412.2:n.1540C>T
|
|
|
ENST00000517643.2:c.484C>T
|
ENSP00000513333.1:p.Arg162Ter
|
|
ENST00000520675.1:c.190C>T
|
ENSP00000428566.1:p.Arg64Ter
|
|
ENST00000521381.5:c.484C>T
|
ENSP00000428056.1:p.Arg162Ter
|
|
ENST00000521657.5:c.484C>T
|
ENSP00000429277.1:p.Arg162Ter
|
|
ENST00000521657.6:c.484C>T
|
ENSP00000429277.1:p.Arg162Ter
|
|
ENST00000697457.1:c.427+513C>T
|
ENSP00000513315.1:n.427+513C>T
|
|
ENST00000697458.1:c.484C>T
|
ENSP00000513316.1:p.Arg162Ter
|
|
ENST00000697460.1:c.-42C>T
|
ENSP00000513318.1:n.-42C>T
|
|
ENST00000697461.1:c.484C>T
|
ENSP00000513319.1:p.Arg162Ter
|
|
ENST00000697556.1:c.391C>T
|
ENSP00000513334.1:p.Arg131Ter
|
|
XM_005248542.2:c.484C>T
|
XP_005248599.1:p.Arg162Ter
|
|
XM_005248542.3:c.484C>T
|
XP_005248599.1:p.Arg162Ter
|
|
XM_011543493.1:c.157C>T
|
XP_011541795.1:p.Arg53Ter
|
|
XM_011543493.3:c.157C>T
|
XP_011541795.1:p.Arg53Ter
|
|
XM_017009585.2:c.484C>T
|
XP_016865074.1:p.Arg162Ter
|
|
XM_017009586.1:c.211C>T
|
XP_016865075.1:p.Arg71Ter
|