|
ENST00000261769.10:c.754G=
MANE Select
|
ENSP00000261769.4:p.Val252=
|
|
|
ENST00000261769.9:c.754G=
|
ENSP00000261769.4:p.Val252=
|
|
|
ENST00000422392.6:c.754G=
|
ENSP00000414946.2:p.Val252=
|
|
|
ENST00000561751.1:c.454+1415G=
|
|
|
|
ENST00000562836.5:n.825G=
|
|
|
|
ENST00000566510.5:c.598G=
|
ENSP00000458139.1:p.Val200=
|
|
|
ENST00000566612.5:c.754G=
|
ENSP00000454782.1:p.Val252=
|
|
|
ENST00000611625.4:c.754G=
|
ENSP00000481063.1:p.Val252=
|
|
|
ENST00000612417.4:c.754G=
|
ENSP00000478360.1:p.Val252=
|
|
|
ENST00000621016.4:c.754G=
|
ENSP00000480664.1:p.Val252=
|
|
|
NM_004360.3:c.754G= , LRG_301t1:c.754G=
|
NP_004351.1:p.Val252=
|
|
|
XM_011523488.1:c.19G=
|
XP_011521790.1:p.Val7=
|
|
|
XM_011523489.1:c.19G=
|
XP_011521791.1:p.Val7=
|
|
|
NM_001317184.1:c.754G=
|
NP_001304113.1:p.Val252=
|
|
|
NM_001317185.1:c.-862G=
|
NP_001304114.1:n.-862G=
|
|
|
NM_001317186.1:c.-1066G=
|
NP_001304115.1:n.-1066G=
|
|
|
NM_004360.4:c.754G=
|
NP_004351.1:p.Val252=
|
|
|
NM_004360.5:c.754G=
MANE Select
|
NP_004351.1:p.Val252=
|
|
|
NM_001317184.2:c.754G=
|
NP_001304113.1:p.Val252=
|
|
|
NM_001317185.2:c.-862G=
|
NP_001304114.1:n.-862G=
|
|
|
NM_001317186.2:c.-1066G=
|
NP_001304115.1:n.-1066G=
|
|
