ENST00000456935.7:c.2760G>T
MANE Select
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ENSP00000395473.2:p.Gln920His
|
|
ENST00000221363.8:c.2757G>T
|
ENSP00000221363.4:p.Gln919His
|
|
ENST00000456935.6:c.2760G>T
|
ENSP00000395473.2:p.Gln920His
|
|
ENST00000466794.5:n.3350G>T
|
|
|
ENST00000469423.1:n.82G>T
|
|
|
ENST00000493218.5:n.171G>T
|
|
|
ENST00000597692.1:c.319G>T
|
|
|
NM_000528.3:c.2760G>T
|
NP_000519.2:p.Gln920His
|
|
NM_001173498.1:c.2757G>T
|
NP_001166969.1:p.Gln919His
|
|
XM_005259913.1:c.2763G>T
|
XP_005259970.1:p.Gln921His
|
|
XM_011528017.1:c.1659G>T
|
XP_011526319.1:p.Gln553His
|
|
XM_005259913.2:c.2763G>T
|
XP_005259970.1:p.Gln921His
|
|
XM_024451518.1:c.1659G>T
|
XP_024307286.1:p.Gln553His
|
|
NM_000528.4:c.2760G>T
MANE Select
|
NP_000519.2:p.Gln920His
|
|
NM_001173498.2:c.2757G>T
|
NP_001166969.1:p.Gln919His
|
|