ENST00000622290.5:c.2964C>G
|
ENSP00000483331.2:p.Gly988=
|
|
ENST00000205557.12:c.2964C>G
MANE Select
|
ENSP00000205557.7:p.Gly988=
|
|
ENST00000205557.11:c.2964C>G
|
ENSP00000205557.7:p.Gly988=
|
|
ENST00000456970.6:c.2789C>G
|
ENSP00000405002.2:n.2789C>G
|
|
ENST00000622290.4:c.*173C>G
|
ENSP00000483331.1:n.*173C>G
|
|
NM_001171.5:c.2964C>G
|
NP_001162.4:p.Gly988=
|
|
XM_011522479.1:c.2931C>G
|
XP_011520781.1:p.Gly977=
|
|
XM_011522480.1:c.2622C>G
|
XP_011520782.1:p.Gly874=
|
|
XM_011522481.1:c.2622C>G
|
XP_011520783.1:p.Gly874=
|
|
XR_932836.1:n.3199C>G
|
|
|
XR_932837.1:n.3200C>G
|
|
|
XR_932838.1:n.3200C>G
|
|
|
NM_001351800.1:c.2622C>G
|
NP_001338729.1:p.Gly874=
|
|
NR_147784.1:n.2826C>G
|
|
|
XM_011522479.2:c.2931C>G
|
XP_011520781.1:p.Gly977=
|
|
XM_011522481.3:c.2622C>G
|
XP_011520783.1:p.Gly874=
|
|
XM_017023212.1:c.2796C>G
|
XP_016878701.1:p.Gly932=
|
|
XM_017023214.1:c.2964C>G
|
XP_016878703.1:p.Gly988=
|
|
XM_024450261.1:c.3000C>G
|
XP_024306029.1:p.Gly1000=
|
|
XR_932836.2:n.3145C>G
|
|
|
XR_932837.3:n.3145C>G
|
|
|
XR_932838.3:n.3145C>G
|
|
|
NM_001171.6:c.2964C>G
MANE Select
|
NP_001162.5:p.Gly988=
|
|