ENST00000703986.1:c.7193C>G
|
ENSP00000515603.1:p.Ala2398Gly
|
|
ENST00000703987.1:c.7193C>G
|
ENSP00000515604.1:p.Ala2398Gly
|
|
ENST00000704649.1:c.3685-3018C>G
|
ENSP00000515974.1:n.3685-3018C>G
|
|
ENST00000704650.1:c.7178C>G
|
ENSP00000515975.1:p.Ala2393Gly
|
|
ENST00000704651.1:c.7025C>G
|
ENSP00000515976.1:p.Ala2342Gly
|
|
ENST00000704652.1:c.6277C>G
|
|
|
ENST00000704654.1:c.4057C>G
|
|
|
ENST00000704655.1:c.3321C>G
|
ENSP00000515980.1:n.3321C>G
|
|
ENST00000704656.1:c.2629C>G
|
ENSP00000515981.1:n.2629C>G
|
|
ENST00000324545.9:c.7178C>G
|
ENSP00000316357.6:p.Ala2393Gly
|
|
ENST00000378308.7:c.7178C>G
MANE Select
|
ENSP00000367558.2:p.Ala2393Gly
|
|
ENST00000324545.8:c.7178C>G
|
ENSP00000316357.6:p.Ala2393Gly
|
|
ENST00000378308.6:c.7178C>G
|
ENSP00000367558.2:p.Ala2393Gly
|
|
ENST00000485180.1:n.387C>G
|
|
|
NM_001039590.2:c.7178C>G
|
NP_001034679.2:p.Ala2393Gly
|
|
NM_001039591.2:c.7178C>G
|
NP_001034680.2:p.Ala2393Gly
|
|
XM_005272675.3:c.7193C>G
|
XP_005272732.1:p.Ala2398Gly
|
|
XM_005272676.3:c.7193C>G
|
XP_005272733.1:p.Ala2398Gly
|
|
XM_005272675.4:c.7193C>G
|
XP_005272732.1:p.Ala2398Gly
|
|
XM_005272676.4:c.7193C>G
|
XP_005272733.1:p.Ala2398Gly
|
|
NM_001039591.3:c.7178C>G
MANE Select
|
NP_001034680.2:p.Ala2393Gly
|
|
NM_001039590.3:c.7178C>G
|
NP_001034679.2:p.Ala2393Gly
|
|