ENST00000622290.5:c.2803C>G
|
ENSP00000483331.2:p.His935Asp
|
|
ENST00000205557.12:c.2803C>G
MANE Select
|
ENSP00000205557.7:p.His935Asp
|
|
ENST00000205557.11:c.2803C>G
|
ENSP00000205557.7:p.His935Asp
|
|
ENST00000456970.6:c.2628C>G
|
ENSP00000405002.2:n.2628C>G
|
|
ENST00000622290.4:c.*12C>G
|
ENSP00000483331.1:n.*12C>G
|
|
NM_001171.5:c.2803C>G
|
NP_001162.4:p.His935Asp
|
|
XM_011522479.1:c.2770C>G
|
XP_011520781.1:p.His924Asp
|
|
XM_011522480.1:c.2461C>G
|
XP_011520782.1:p.His821Asp
|
|
XM_011522481.1:c.2461C>G
|
XP_011520783.1:p.His821Asp
|
|
XR_932836.1:n.3038C>G
|
|
|
XR_932837.1:n.3039C>G
|
|
|
XR_932838.1:n.3039C>G
|
|
|
NM_001351800.1:c.2461C>G
|
NP_001338729.1:p.His821Asp
|
|
NR_147784.1:n.2665C>G
|
|
|
XM_011522479.2:c.2770C>G
|
XP_011520781.1:p.His924Asp
|
|
XM_011522481.3:c.2461C>G
|
XP_011520783.1:p.His821Asp
|
|
XM_017023212.1:c.2635C>G
|
XP_016878701.1:p.His879Asp
|
|
XM_017023214.1:c.2803C>G
|
XP_016878703.1:p.His935Asp
|
|
XM_024450261.1:c.2839C>G
|
XP_024306029.1:p.His947Asp
|
|
XR_932836.2:n.2984C>G
|
|
|
XR_932837.3:n.2984C>G
|
|
|
XR_932838.3:n.2984C>G
|
|
|
NM_001171.6:c.2803C>G
MANE Select
|
NP_001162.5:p.His935Asp
|
|