ENST00000370096.9:c.2725G=
MANE Select
|
ENSP00000359114.3:p.Asp909=
|
|
ENST00000353414.8:c.2608G=
|
ENSP00000302551.6:p.Asp870=
|
|
ENST00000358392.6:c.2761G=
|
ENSP00000351163.2:p.Asp921=
|
|
ENST00000370096.7:c.2725G=
|
ENSP00000359114.3:p.Asp909=
|
|
ENST00000512756.5:c.2377G=
|
ENSP00000426533.1:p.Asp793=
|
|
ENST00000635193.1:c.2059G=
|
|
|
NM_001190709.1:c.2608G=
|
NP_001177638.1:p.Asp870=
|
|
NM_001854.3:c.2725G=
|
NP_001845.3:p.Asp909=
|
|
NM_080629.2:c.2761G=
|
NP_542196.2:p.Asp921=
|
|
NM_080630.3:c.2377G=
|
NP_542197.3:p.Asp793=
|
|
XM_011540719.1:c.2725G=
|
XP_011539021.1:p.Asp909=
|
|
XM_011540720.1:c.958G=
|
XP_011539022.1:p.Asp320=
|
|
XM_011540721.1:c.313G=
|
XP_011539023.1:p.Asp105=
|
|
XR_946545.1:n.3139G=
|
|
|
NR_134980.1:n.3059G=
|
|
|
XM_017000334.1:c.2878G=
|
XP_016855823.1:p.Asp960=
|
|
XM_017000335.1:c.2872G=
|
XP_016855824.1:p.Asp958=
|
|
XM_017000336.1:c.2878G=
|
XP_016855825.1:p.Asp960=
|
|
XM_017000337.1:c.1276G=
|
XP_016855826.1:p.Asp426=
|
|
NM_001854.4:c.2725G=
MANE Select
|
NP_001845.3:p.Asp909=
|
|
NM_080630.4:c.2377G=
|
NP_542197.3:p.Asp793=
|
|
NR_134980.2:n.3085G=
|
|
|
NM_001190709.2:c.2608G=
|
NP_001177638.1:p.Asp870=
|
|
NM_080629.3:c.2761G=
|
NP_542196.2:p.Asp921=
|
|