ENST00000370096.9:c.3264G=
MANE Select
|
ENSP00000359114.3:p.Glu1088=
|
|
ENST00000353414.8:c.3147G=
|
ENSP00000302551.6:p.Glu1049=
|
|
ENST00000358392.6:c.3300G=
|
ENSP00000351163.2:p.Glu1100=
|
|
ENST00000370096.7:c.3264G=
|
ENSP00000359114.3:p.Glu1088=
|
|
ENST00000512756.5:c.2916G=
|
ENSP00000426533.1:p.Glu972=
|
|
ENST00000635193.1:c.2598G=
|
|
|
NM_001190709.1:c.3147G=
|
NP_001177638.1:p.Glu1049=
|
|
NM_001854.3:c.3264G=
|
NP_001845.3:p.Glu1088=
|
|
NM_080629.2:c.3300G=
|
NP_542196.2:p.Glu1100=
|
|
NM_080630.3:c.2916G=
|
NP_542197.3:p.Glu972=
|
|
XM_011540719.1:c.3264G=
|
XP_011539021.1:p.Glu1088=
|
|
XM_011540720.1:c.1497G=
|
XP_011539022.1:p.Glu499=
|
|
XM_011540721.1:c.852G=
|
XP_011539023.1:p.Glu284=
|
|
NR_134980.1:n.3598G=
|
|
|
XM_017000334.1:c.3417G=
|
XP_016855823.1:p.Glu1139=
|
|
XM_017000335.1:c.3411G=
|
XP_016855824.1:p.Glu1137=
|
|
XM_017000336.1:c.3417G=
|
XP_016855825.1:p.Glu1139=
|
|
XM_017000337.1:c.1815G=
|
XP_016855826.1:p.Glu605=
|
|
NM_001854.4:c.3264G=
MANE Select
|
NP_001845.3:p.Glu1088=
|
|
NM_080630.4:c.2916G=
|
NP_542197.3:p.Glu972=
|
|
NR_134980.2:n.3624G=
|
|
|
NM_001190709.2:c.3147G=
|
NP_001177638.1:p.Glu1049=
|
|
NM_080629.3:c.3300G=
|
NP_542196.2:p.Glu1100=
|
|