|
NM_181523.3:c.901C>T
MANE Select
|
NP_852664.1:p.Arg301Ter
|
|
ENST00000521381.6:c.901C>T
MANE Select
|
ENSP00000428056.1:p.Arg301Ter
|
|
NM_181523.2:c.901C>T
|
NP_852664.1:p.Arg301Ter
|
|
ENST00000517643.2:c.901C>T
|
ENSP00000513333.1:p.Arg301Ter
|
|
ENST00000521381.5:c.901C>T
|
ENSP00000428056.1:p.Arg301Ter
|
|
ENST00000521657.5:c.901C>T
|
ENSP00000429277.1:p.Arg301Ter
|
|
ENST00000521657.6:c.901C>T
|
ENSP00000429277.1:p.Arg301Ter
|
|
ENST00000522084.5:c.91C>T
|
ENSP00000429766.1:p.Arg31Ter
|
|
ENST00000522084.6:c.91C>T
|
ENSP00000429766.2:p.Arg31Ter
|
|
ENST00000523807.5:c.91C>T
|
ENSP00000430126.1:p.Arg31Ter
|
|
ENST00000697457.1:c.826C>T
|
ENSP00000513315.1:p.Arg276Ter
|
|
ENST00000697458.1:c.901C>T
|
ENSP00000513316.1:p.Arg301Ter
|
|
ENST00000697460.1:c.376C>T
|
ENSP00000513318.1:p.Arg126Ter
|
|
ENST00000697461.1:c.901C>T
|
ENSP00000513319.1:p.Arg301Ter
|
|
ENST00000697556.1:c.808C>T
|
ENSP00000513334.1:p.Arg270Ter
|
|
XM_005248542.2:c.901C>T
|
XP_005248599.1:p.Arg301Ter
|
|
XM_005248542.3:c.901C>T
|
XP_005248599.1:p.Arg301Ter
|
|
XM_011543493.1:c.574C>T
|
XP_011541795.1:p.Arg192Ter
|
|
XM_011543493.3:c.574C>T
|
XP_011541795.1:p.Arg192Ter
|
|
XM_017009585.2:c.901C>T
|
XP_016865074.1:p.Arg301Ter
|
|
XM_017009586.1:c.628C>T
|
XP_016865075.1:p.Arg210Ter
|