ENST00000456935.7:c.1122T>G
MANE Select
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ENSP00000395473.2:p.His374Gln
|
|
ENST00000221363.8:c.1119T>G
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ENSP00000221363.4:p.His373Gln
|
|
ENST00000456935.6:c.1122T>G
|
ENSP00000395473.2:p.His374Gln
|
|
ENST00000465830.1:n.286T>G
|
|
|
ENST00000466794.5:n.1021T>G
|
|
|
ENST00000495617.1:n.280+399T>G
|
|
|
NM_000528.3:c.1122T>G
|
NP_000519.2:p.His374Gln
|
|
NM_001173498.1:c.1119T>G
|
NP_001166969.1:p.His373Gln
|
|
XM_005259913.1:c.1125T>G
|
XP_005259970.1:p.His375Gln
|
|
XM_011528017.1:c.21T>G
|
XP_011526319.1:p.His7Gln
|
|
XM_005259913.2:c.1125T>G
|
XP_005259970.1:p.His375Gln
|
|
XM_024451518.1:c.21T>G
|
XP_024307286.1:p.His7Gln
|
|
NM_000528.4:c.1122T>G
MANE Select
|
NP_000519.2:p.His374Gln
|
|
NM_001173498.2:c.1119T>G
|
NP_001166969.1:p.His373Gln
|
|