ENST00000456935.7:c.1155C>G
MANE Select
|
ENSP00000395473.2:p.His385Gln
|
|
ENST00000221363.8:c.1152C>G
|
ENSP00000221363.4:p.His384Gln
|
|
ENST00000456935.6:c.1155C>G
|
ENSP00000395473.2:p.His385Gln
|
|
ENST00000465830.1:n.319C>G
|
|
|
ENST00000466794.5:n.1054C>G
|
|
|
ENST00000495617.1:n.280+432C>G
|
|
|
NM_000528.3:c.1155C>G
|
NP_000519.2:p.His385Gln
|
|
NM_001173498.1:c.1152C>G
|
NP_001166969.1:p.His384Gln
|
|
XM_005259913.1:c.1158C>G
|
XP_005259970.1:p.His386Gln
|
|
XM_011528017.1:c.54C>G
|
XP_011526319.1:p.His18Gln
|
|
XM_005259913.2:c.1158C>G
|
XP_005259970.1:p.His386Gln
|
|
XM_024451518.1:c.54C>G
|
XP_024307286.1:p.His18Gln
|
|
NM_000528.4:c.1155C>G
MANE Select
|
NP_000519.2:p.His385Gln
|
|
NM_001173498.2:c.1152C>G
|
NP_001166969.1:p.His384Gln
|
|