ENST00000389857.11:c.925C>G
MANE Select
|
ENSP00000374507.6:p.Arg309Gly
|
|
ENST00000389857.10:c.925C>G
|
ENSP00000374507.6:p.Arg309Gly
|
|
ENST00000554051.1:n.402C>G
|
|
|
NM_001080414.3:c.925C>G
|
NP_001073883.2:p.Arg309Gly
|
|
XM_005267691.3:c.925C>G
|
XP_005267748.1:p.Arg309Gly
|
|
XM_011536796.1:c.817C>G
|
XP_011535098.1:p.Arg273Gly
|
|
XR_429316.2:n.1053C>G
|
|
|
XR_943459.1:n.1053C>G
|
|
|
XM_005267691.5:c.925C>G
|
XP_005267748.1:p.Arg309Gly
|
|
XM_011536796.2:c.817C>G
|
XP_011535098.1:p.Arg273Gly
|
|
XM_017021335.2:c.925C>G
|
XP_016876824.1:p.Arg309Gly
|
|
XM_017021337.2:c.925C>G
|
XP_016876826.1:p.Arg309Gly
|
|
XR_429316.4:n.1051C>G
|
|
|
NM_001080414.4:c.925C>G
MANE Select
|
NP_001073883.2:p.Arg309Gly
|
|