ENST00000409383.6:c.886G>T
|
ENSP00000386346.2:p.Asp296Tyr
|
|
ENST00000519937.7:c.886G>T
MANE Select
|
ENSP00000428719.2:p.Asp296Tyr
|
|
ENST00000393822.7:c.886G>T
|
ENSP00000377409.4:p.Asp296Tyr
|
|
ENST00000409383.5:c.922G>T
|
ENSP00000386346.1:p.Asp308Tyr
|
|
ENST00000428225.5:c.863G>T
|
|
|
ENST00000491167.1:n.86G>T
|
|
|
ENST00000494165.1:c.17G>T
|
|
|
ENST00000519937.6:c.886G>T
|
ENSP00000428719.2:p.Asp296Tyr
|
|
NM_000542.3:c.922G>T
|
NP_000533.3:p.Asp308Tyr
|
|
NM_198843.2:c.922G>T
|
NP_942140.2:p.Asp308Tyr
|
|
XM_005264487.2:c.922G>T
|
XP_005264544.1:p.Asp308Tyr
|
|
XM_005264488.2:c.874G>T
|
XP_005264545.2:p.Asp292Tyr
|
|
XM_005264490.3:c.886G>T
|
XP_005264547.2:p.Asp296Tyr
|
|
XM_005264488.4:c.874G>T
|
XP_005264545.2:p.Asp292Tyr
|
|
XM_005264490.4:c.886G>T
|
XP_005264547.2:p.Asp296Tyr
|
|
NM_000542.4:c.886G>T
|
NP_000533.4:p.Asp296Tyr
|
|
NM_001367281.1:c.886G>T
|
NP_001354210.1:p.Asp296Tyr
|
|
NM_198843.3:c.886G>T
|
NP_942140.3:p.Asp296Tyr
|
|
NM_000542.5:c.886G>T
MANE Select
|
NP_000533.4:p.Asp296Tyr
|
|