ENST00000352511.5:c.961G>T
MANE Select
|
ENSP00000340361.3:p.Asp321Tyr
|
|
ENST00000352511.4:c.961G>T
|
ENSP00000340361.3:p.Asp321Tyr
|
|
ENST00000461232.1:n.4750G>T
|
|
|
ENST00000465020.5:n.1047G>T
|
|
|
NM_001106.3:c.961G>T
|
NP_001097.2:p.Asp321Tyr
|
|
XM_005265583.2:c.1024G>T
|
XP_005265640.1:p.Asp342Tyr
|
|
XM_005265583.3:c.1024G>T
|
XP_005265640.1:p.Asp342Tyr
|
|
XM_017007514.1:c.1003G>T
|
XP_016863003.1:p.Asp335Tyr
|
|
XM_017007515.2:c.979G>T
|
XP_016863004.1:p.Asp327Tyr
|
|
XM_017007516.1:c.958G>T
|
XP_016863005.1:p.Asp320Tyr
|
|
NM_001106.4:c.961G>T
MANE Select
|
NP_001097.2:p.Asp321Tyr
|
|