|
ENST00000261769.10:c.2420T=
MANE Select
|
ENSP00000261769.4:p.Ile807=
|
|
|
ENST00000261769.9:c.2420T=
|
ENSP00000261769.4:p.Ile807=
|
|
|
ENST00000422392.6:c.2237T=
|
ENSP00000414946.2:p.Ile746=
|
|
|
ENST00000562118.1:n.638T=
|
|
|
|
ENST00000562836.5:n.2491T=
|
|
|
|
ENST00000566510.5:c.*1086T=
|
ENSP00000458139.1:n.*1086T=
|
|
|
ENST00000566612.5:c.*660T=
|
ENSP00000454782.1:n.*660T=
|
|
|
ENST00000611625.4:c.2483T=
|
ENSP00000481063.1:p.Ile828=
|
|
|
ENST00000612417.4:c.1853+3224T=
|
ENSP00000478360.1:n.1853+3224T=
|
|
|
ENST00000621016.4:c.1866-4425T=
|
ENSP00000480664.1:n.1866-4425T=
|
|
|
NM_004360.3:c.2420T= , LRG_301t1:c.2420T=
|
NP_004351.1:p.Ile807=
|
|
|
XM_011523488.1:c.1685T=
|
XP_011521790.1:p.Ile562=
|
|
|
XM_011523489.1:c.1685T=
|
XP_011521791.1:p.Ile562=
|
|
|
NM_001317184.1:c.2237T=
|
NP_001304113.1:p.Ile746=
|
|
|
NM_001317185.1:c.872T=
|
NP_001304114.1:p.Ile291=
|
|
|
NM_001317186.1:c.455T=
|
NP_001304115.1:p.Ile152=
|
|
|
NM_004360.4:c.2420T=
|
NP_004351.1:p.Ile807=
|
|
|
NM_004360.5:c.2420T=
MANE Select
|
NP_004351.1:p.Ile807=
|
|
|
NM_001317184.2:c.2237T=
|
NP_001304113.1:p.Ile746=
|
|
|
NM_001317185.2:c.872T=
|
NP_001304114.1:p.Ile291=
|
|
|
NM_001317186.2:c.455T=
|
NP_001304115.1:p.Ile152=
|
|
