ENST00000321867.6:c.2757C>G
MANE Select
|
ENSP00000324560.3:p.Asp919Glu
|
|
ENST00000321867.5:c.2757C>G
|
ENSP00000324560.3:p.Asp919Glu
|
|
ENST00000540647.5:n.626C>G
|
|
|
ENST00000544718.1:n.304C>G
|
|
|
NM_003565.2:c.2757C>G
|
NP_003556.1:p.Asp919Glu
|
|
XM_011538798.1:c.2826C>G
|
XP_011537100.1:p.Asp942Glu
|
|
XM_011538799.1:c.2739C>G
|
XP_011537101.1:p.Asp913Glu
|
|
XR_944753.1:n.2539C>G
|
|
|
XM_011538798.3:c.2826C>G
|
XP_011537100.1:p.Asp942Glu
|
|
XM_011538799.2:c.2739C>G
|
XP_011537101.1:p.Asp913Glu
|
|
XR_001748883.2:n.2545C>G
|
|
|
NM_003565.3:c.2757C>G
|
NP_003556.1:p.Asp919Glu
|
|
NM_003565.4:c.2757C>G
MANE Select
|
NP_003556.2:p.Asp919Glu
|
|