|
ENST00000261769.10:c.2352T=
MANE Select
|
ENSP00000261769.4:p.Arg784=
|
|
|
ENST00000261769.9:c.2352T=
|
ENSP00000261769.4:p.Arg784=
|
|
|
ENST00000422392.6:c.2169T=
|
ENSP00000414946.2:p.Arg723=
|
|
|
ENST00000562118.1:n.570T=
|
|
|
|
ENST00000562836.5:n.2423T=
|
|
|
|
ENST00000566510.5:c.*1018T=
|
ENSP00000458139.1:n.*1018T=
|
|
|
ENST00000566612.5:c.*592T=
|
ENSP00000454782.1:n.*592T=
|
|
|
ENST00000611625.4:c.2415T=
|
ENSP00000481063.1:p.Arg805=
|
|
|
ENST00000612417.4:c.1853+3156T=
|
ENSP00000478360.1:n.1853+3156T=
|
|
|
ENST00000621016.4:c.1866-4493T=
|
ENSP00000480664.1:n.1866-4493T=
|
|
|
NM_004360.3:c.2352T= , LRG_301t1:c.2352T=
|
NP_004351.1:p.Arg784=
|
|
|
XM_011523488.1:c.1617T=
|
XP_011521790.1:p.Arg539=
|
|
|
XM_011523489.1:c.1617T=
|
XP_011521791.1:p.Arg539=
|
|
|
NM_001317184.1:c.2169T=
|
NP_001304113.1:p.Arg723=
|
|
|
NM_001317185.1:c.804T=
|
NP_001304114.1:p.Arg268=
|
|
|
NM_001317186.1:c.387T=
|
NP_001304115.1:p.Arg129=
|
|
|
NM_004360.4:c.2352T=
|
NP_004351.1:p.Arg784=
|
|
|
NM_004360.5:c.2352T=
MANE Select
|
NP_004351.1:p.Arg784=
|
|
|
NM_001317184.2:c.2169T=
|
NP_001304113.1:p.Arg723=
|
|
|
NM_001317185.2:c.804T=
|
NP_001304114.1:p.Arg268=
|
|
|
NM_001317186.2:c.387T=
|
NP_001304115.1:p.Arg129=
|
|
