ENST00000622290.5:c.*662C>G
|
ENSP00000483331.2:n.*662C>G
|
|
ENST00000205557.12:c.4490C>G
MANE Select
|
ENSP00000205557.7:p.Ala1497Gly
|
|
ENST00000640696.1:c.1304C>G
|
ENSP00000492197.1:p.Ala435Gly
|
|
ENST00000205557.11:c.4490C>G
|
ENSP00000205557.7:p.Ala1497Gly
|
|
ENST00000456970.6:c.4115C>G
|
ENSP00000405002.2:n.4115C>G
|
|
ENST00000576204.5:n.1353C>G
|
|
|
ENST00000622290.4:c.*1699C>G
|
ENSP00000483331.1:n.*1699C>G
|
|
NM_001171.5:c.4490C>G
|
NP_001162.4:p.Ala1497Gly
|
|
XM_011522479.1:c.4457C>G
|
XP_011520781.1:p.Ala1486Gly
|
|
XM_011522480.1:c.4148C>G
|
XP_011520782.1:p.Ala1383Gly
|
|
XM_011522481.1:c.4148C>G
|
XP_011520783.1:p.Ala1383Gly
|
|
XR_933134.1:n.538+5865G>C
|
|
|
NM_001351800.1:c.4148C>G
|
NP_001338729.1:p.Ala1383Gly
|
|
NR_147784.1:n.4152C>G
|
|
|
XM_011522479.2:c.4457C>G
|
XP_011520781.1:p.Ala1486Gly
|
|
XM_011522481.3:c.4148C>G
|
XP_011520783.1:p.Ala1383Gly
|
|
XM_017023212.1:c.4322C>G
|
XP_016878701.1:p.Ala1441Gly
|
|
XM_024450261.1:c.4526C>G
|
XP_024306029.1:p.Ala1509Gly
|
|
NM_001171.6:c.4490C>G
MANE Select
|
NP_001162.5:p.Ala1497Gly
|
|