ENST00000682568.1:n.1811T>G
|
|
|
ENST00000682617.1:c.1871T>G
|
ENSP00000507912.1:p.Val624Gly
|
|
ENST00000682826.1:c.*1047T>G
|
ENSP00000507274.1:n.*1047T>G
|
|
ENST00000682909.1:n.3773T>G
|
|
|
ENST00000683277.1:n.3378T>G
|
|
|
ENST00000683407.1:n.1741T>G
|
|
|
ENST00000683962.1:c.*1427T>G
|
ENSP00000506854.1:n.*1427T>G
|
|
ENST00000311895.8:c.1733T>G
MANE Select
|
ENSP00000310520.7:p.Val578Gly
|
|
ENST00000311895.7:c.1733T>G
|
ENSP00000310520.7:p.Val578Gly
|
|
ENST00000389138.7:n.1010T>G
|
|
|
NM_005236.2:c.1733T>G , LRG_463t1:c.1733T>G
|
NP_005227.1:p.Val578Gly
|
|
XM_011522424.1:c.1871T>G
|
XP_011520726.1:p.Val624Gly
|
|
XM_011522425.1:c.1190T>G
|
XP_011520727.1:p.Val397Gly
|
|
XM_011522426.1:c.944T>G
|
XP_011520728.1:p.Val315Gly
|
|
XM_011522427.1:c.383T>G
|
XP_011520729.1:p.Val128Gly
|
|
XR_932805.1:n.1892T>G
|
|
|
XM_011522424.3:c.1871T>G
|
XP_011520726.1:p.Val624Gly
|
|
XM_017023043.2:c.944T>G
|
XP_016878532.1:p.Val315Gly
|
|
NM_005236.3:c.1733T>G
MANE Select
|
NP_005227.1:p.Val578Gly
|
|