ENST00000261769.10:c.1983T=
MANE Select
|
ENSP00000261769.4:p.Gly661=
|
|
ENST00000261769.9:c.1983T=
|
ENSP00000261769.4:p.Gly661=
|
|
ENST00000422392.6:c.1800T=
|
ENSP00000414946.2:p.Gly600=
|
|
ENST00000562118.1:n.201T=
|
|
|
ENST00000562836.5:n.2054T=
|
|
|
ENST00000566510.5:c.*649T=
|
ENSP00000458139.1:n.*649T=
|
|
ENST00000566612.5:c.*223T=
|
ENSP00000454782.1:n.*223T=
|
|
ENST00000611625.4:c.2046T=
|
ENSP00000481063.1:p.Gly682=
|
|
ENST00000612417.4:c.1830+1326T=
|
ENSP00000478360.1:n.1830+1326T=
|
|
ENST00000621016.4:c.1865+1291T=
|
ENSP00000480664.1:n.1865+1291T=
|
|
NM_004360.3:c.1983T= , LRG_301t1:c.1983T=
|
NP_004351.1:p.Gly661=
|
|
XM_011523488.1:c.1248T=
|
XP_011521790.1:p.Gly416=
|
|
XM_011523489.1:c.1248T=
|
XP_011521791.1:p.Gly416=
|
|
NM_001317184.1:c.1800T=
|
NP_001304113.1:p.Gly600=
|
|
NM_001317185.1:c.435T=
|
NP_001304114.1:p.Gly145=
|
|
NM_001317186.1:c.18T=
|
NP_001304115.1:p.Gly6=
|
|
NM_004360.4:c.1983T=
|
NP_004351.1:p.Gly661=
|
|
NM_004360.5:c.1983T=
MANE Select
|
NP_004351.1:p.Gly661=
|
|
NM_001317184.2:c.1800T=
|
NP_001304113.1:p.Gly600=
|
|
NM_001317185.2:c.435T=
|
NP_001304114.1:p.Gly145=
|
|
NM_001317186.2:c.18T=
|
NP_001304115.1:p.Gly6=
|
|