ENST00000456935.7:c.2701C>G
MANE Select
|
ENSP00000395473.2:p.His901Asp
|
|
ENST00000221363.8:c.2698C>G
|
ENSP00000221363.4:p.His900Asp
|
|
ENST00000456935.6:c.2701C>G
|
ENSP00000395473.2:p.His901Asp
|
|
ENST00000466794.5:n.3291C>G
|
|
|
ENST00000469423.1:n.23C>G
|
|
|
ENST00000493218.5:n.112C>G
|
|
|
ENST00000597692.1:c.260C>G
|
|
|
NM_000528.3:c.2701C>G
|
NP_000519.2:p.His901Asp
|
|
NM_001173498.1:c.2698C>G
|
NP_001166969.1:p.His900Asp
|
|
XM_005259913.1:c.2704C>G
|
XP_005259970.1:p.His902Asp
|
|
XM_011528017.1:c.1600C>G
|
XP_011526319.1:p.His534Asp
|
|
XM_005259913.2:c.2704C>G
|
XP_005259970.1:p.His902Asp
|
|
XM_024451518.1:c.1600C>G
|
XP_024307286.1:p.His534Asp
|
|
NM_000528.4:c.2701C>G
MANE Select
|
NP_000519.2:p.His901Asp
|
|
NM_001173498.2:c.2698C>G
|
NP_001166969.1:p.His900Asp
|
|