|
ENST00000261769.10:c.729G>A
MANE Select
|
ENSP00000261769.4:p.Glu243=
|
|
|
ENST00000261769.9:c.729G>A
|
ENSP00000261769.4:p.Glu243=
|
|
|
ENST00000422392.6:c.729G>A
|
ENSP00000414946.2:p.Glu243=
|
|
|
ENST00000561751.1:c.454+1390G>A
|
|
|
|
ENST00000562836.5:n.800G>A
|
|
|
|
ENST00000566510.5:c.573G>A
|
ENSP00000458139.1:p.Glu191=
|
|
|
ENST00000566612.5:c.729G>A
|
ENSP00000454782.1:p.Glu243=
|
|
|
ENST00000611625.4:c.729G>A
|
ENSP00000481063.1:p.Glu243=
|
|
|
ENST00000612417.4:c.729G>A
|
ENSP00000478360.1:p.Glu243=
|
|
|
ENST00000621016.4:c.729G>A
|
ENSP00000480664.1:p.Glu243=
|
|
|
NM_004360.3:c.729G>A , LRG_301t1:c.729G>A
|
NP_004351.1:p.Glu243=
|
|
|
XM_011523488.1:c.-7G>A
|
XP_011521790.1:n.-7G>A
|
|
|
XM_011523489.1:c.-7G>A
|
XP_011521791.1:n.-7G>A
|
|
|
NM_001317184.1:c.729G>A
|
NP_001304113.1:p.Glu243=
|
|
|
NM_001317185.1:c.-887G>A
|
NP_001304114.1:n.-887G>A
|
|
|
NM_001317186.1:c.-1091G>A
|
NP_001304115.1:n.-1091G>A
|
|
|
NM_004360.4:c.729G>A
|
NP_004351.1:p.Glu243=
|
|
|
NM_004360.5:c.729G>A
MANE Select
|
NP_004351.1:p.Glu243=
|
|
|
NM_001317184.2:c.729G>A
|
NP_001304113.1:p.Glu243=
|
|
|
NM_001317185.2:c.-887G>A
|
NP_001304114.1:n.-887G>A
|
|
|
NM_001317186.2:c.-1091G>A
|
NP_001304115.1:n.-1091G>A
|
|
