ENST00000529510.6:n.738C>G
|
|
|
ENST00000697845.1:n.662C>G
|
|
|
ENST00000697846.1:n.738C>G
|
|
|
ENST00000697847.1:n.738C>G
|
|
|
ENST00000697848.1:n.738C>G
|
|
|
ENST00000697849.1:n.1777C>G
|
|
|
ENST00000697850.1:n.738C>G
|
|
|
ENST00000697851.1:n.2098C>G
|
|
|
ENST00000638186.1:n.812C>G
|
|
|
ENST00000638360.1:n.644C>G
|
|
|
ENST00000638925.1:n.745C>G
|
|
|
ENST00000650539.1:n.914C>G
|
|
|
ENST00000330775.9:c.509C>G
|
ENSP00000476242.2:p.Ala170Gly
|
|
ENST00000357590.9:c.509C>G
|
ENSP00000476176.2:p.Ala170Gly
|
|
ENST00000524428.5:n.830C>G
|
|
|
ENST00000525039.5:n.932C>G
|
|
|
ENST00000525102.5:n.1266C>G
|
|
|
ENST00000525372.5:n.509C>G
|
|
|
ENST00000526275.5:n.1290C>G
|
|
|
ENST00000526626.6:n.471C>G
|
|
|
ENST00000527992.5:n.736C>G
|
|
|
ENST00000529510.5:n.399+449C>G
|
|
|
ENST00000530407.5:n.658C>G
|
|
|
ENST00000532085.1:n.3119C>G
|
|
|
ENST00000532888.6:n.804C>G
|
|
|
ENST00000538950.5:c.290C>G
|
ENSP00000475991.2:p.Ala97Gly
|
|
ENST00000545985.5:c.509C>G
|
ENSP00000475241.2:p.Ala170Gly
|
|
NM_001164277.1:c.509C>G , LRG_187t1:c.509C>G
|
NP_001157749.1:p.Ala170Gly
|
|
NM_001164278.1:c.509C>G
|
NP_001157750.1:p.Ala170Gly
|
|
NM_001164279.1:c.290C>G
|
NP_001157751.1:p.Ala97Gly
|
|
NM_001164280.1:c.509C>G
|
NP_001157752.1:p.Ala170Gly
|
|
NM_001467.5:c.509C>G
|
NP_001458.1:p.Ala170Gly
|
|
NM_001164278.2:c.509C>G
|
NP_001157750.1:p.Ala170Gly
|
|
NM_001164279.2:c.290C>G
|
NP_001157751.1:p.Ala97Gly
|
|
NM_001164280.2:c.509C>G
|
NP_001157752.1:p.Ala170Gly
|
|
NM_001467.6:c.509C>G
|
NP_001458.1:p.Ala170Gly
|
|
NM_001164277.2:c.509C>G
MANE Select
|
NP_001157749.1:p.Ala170Gly
|
|