ENST00000682617.1:c.2711T>G
|
ENSP00000507912.1:p.Val904Gly
|
|
ENST00000683962.1:c.*2267T>G
|
ENSP00000506854.1:n.*2267T>G
|
|
ENST00000311895.8:c.2573T>G
MANE Select
|
ENSP00000310520.7:p.Val858Gly
|
|
ENST00000311895.7:c.2573T>G
|
ENSP00000310520.7:p.Val858Gly
|
|
ENST00000389138.7:n.1850T>G
|
|
|
NM_005236.2:c.2573T>G , LRG_463t1:c.2573T>G
|
NP_005227.1:p.Val858Gly
|
|
XM_011522424.1:c.2711T>G
|
XP_011520726.1:p.Val904Gly
|
|
XM_011522425.1:c.2030T>G
|
XP_011520727.1:p.Val677Gly
|
|
XM_011522426.1:c.1784T>G
|
XP_011520728.1:p.Val595Gly
|
|
XM_011522427.1:c.1223T>G
|
XP_011520729.1:p.Val408Gly
|
|
XR_932805.1:n.2732T>G
|
|
|
XM_011522424.3:c.2711T>G
|
XP_011520726.1:p.Val904Gly
|
|
XM_017023043.2:c.1784T>G
|
XP_016878532.1:p.Val595Gly
|
|
NM_005236.3:c.2573T>G
MANE Select
|
NP_005227.1:p.Val858Gly
|
|