ENST00000422737.7:c.4652C>G
|
ENSP00000415650.3:p.Ala1551Gly
|
|
ENST00000457135.2:c.861C>G
|
|
|
ENST00000334344.11:c.4652C>G
MANE Select
|
ENSP00000335044.6:p.Ala1551Gly
|
|
ENST00000422737.6:c.4573C>G
|
|
|
ENST00000334344.10:c.4652C>G
|
ENSP00000335044.6:p.Ala1551Gly
|
|
ENST00000422737.5:c.4205C>G
|
ENSP00000415650.1:p.Ala1402Gly
|
|
ENST00000444670.5:c.3482C>G
|
ENSP00000397307.1:p.Ala1161Gly
|
|
ENST00000457135.1:c.476C>G
|
ENSP00000388357.1:p.Ala159Gly
|
|
ENST00000479608.5:n.3943C>G
|
|
|
NM_152641.2:c.4652C>G
|
NP_689854.2:p.Ala1551Gly
|
|
XM_006719272.2:c.4652C>G
|
XP_006719335.1:p.Ala1551Gly
|
|
XM_011538025.1:c.3020C>G
|
XP_011536327.1:p.Ala1007Gly
|
|
XR_944505.1:n.4800C>G
|
|
|
NM_001347839.1:c.4652C>G
|
NP_001334768.1:p.Ala1551Gly
|
|
NM_152641.3:c.4652C>G
|
NP_689854.2:p.Ala1551Gly
|
|
XM_006719272.4:c.4652C>G
|
XP_006719335.1:p.Ala1551Gly
|
|
XR_944505.3:n.4783C>G
|
|
|
NM_152641.4:c.4652C>G
MANE Select
|
NP_689854.2:p.Ala1551Gly
|
|
NM_001347839.2:c.4652C>G
|
NP_001334768.1:p.Ala1551Gly
|
|