ENST00000409383.6:c.957G>T
|
ENSP00000386346.2:p.Gln319His
|
|
ENST00000519937.7:c.957G>T
MANE Select
|
ENSP00000428719.2:p.Gln319His
|
|
ENST00000393822.7:c.957G>T
|
ENSP00000377409.4:p.Gln319His
|
|
ENST00000409383.5:c.993G>T
|
ENSP00000386346.1:p.Gln331His
|
|
ENST00000428225.5:c.934G>T
|
|
|
ENST00000491167.1:n.157G>T
|
|
|
ENST00000494165.1:c.88G>T
|
|
|
ENST00000519937.6:c.957G>T
|
ENSP00000428719.2:p.Gln319His
|
|
NM_000542.3:c.993G>T
|
NP_000533.3:p.Gln331His
|
|
NM_198843.2:c.993G>T
|
NP_942140.2:p.Gln331His
|
|
XM_005264487.2:c.993G>T
|
XP_005264544.1:p.Gln331His
|
|
XM_005264488.2:c.945G>T
|
XP_005264545.2:p.Gln315His
|
|
XM_005264490.3:c.957G>T
|
XP_005264547.2:p.Gln319His
|
|
XM_005264488.4:c.945G>T
|
XP_005264545.2:p.Gln315His
|
|
XM_005264490.4:c.957G>T
|
XP_005264547.2:p.Gln319His
|
|
NM_000542.4:c.957G>T
|
NP_000533.4:p.Gln319His
|
|
NM_001367281.1:c.957G>T
|
NP_001354210.1:p.Gln319His
|
|
NM_198843.3:c.957G>T
|
NP_942140.3:p.Gln319His
|
|
NM_000542.5:c.957G>T
MANE Select
|
NP_000533.4:p.Gln319His
|
|