ENST00000682617.1:c.2143A>G
|
ENSP00000507912.1:p.Thr715Ala
|
|
ENST00000683962.1:c.*1699A>G
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ENSP00000506854.1:n.*1699A>G
|
|
ENST00000311895.8:c.2005A>G
MANE Select
|
ENSP00000310520.7:p.Thr669Ala
|
|
ENST00000311895.7:c.2005A>G
|
ENSP00000310520.7:p.Thr669Ala
|
|
ENST00000389138.7:n.1282A>G
|
|
|
ENST00000462862.1:c.318A>G
|
ENSP00000461322.1:n.318A>G
|
|
NM_005236.2:c.2005A>G , LRG_463t1:c.2005A>G
|
NP_005227.1:p.Thr669Ala
|
|
XM_011522424.1:c.2143A>G
|
XP_011520726.1:p.Thr715Ala
|
|
XM_011522425.1:c.1462A>G
|
XP_011520727.1:p.Thr488Ala
|
|
XM_011522426.1:c.1216A>G
|
XP_011520728.1:p.Thr406Ala
|
|
XM_011522427.1:c.655A>G
|
XP_011520729.1:p.Thr219Ala
|
|
XR_932805.1:n.2164A>G
|
|
|
XM_011522424.3:c.2143A>G
|
XP_011520726.1:p.Thr715Ala
|
|
XM_017023043.2:c.1216A>G
|
XP_016878532.1:p.Thr406Ala
|
|
NM_005236.3:c.2005A>G
MANE Select
|
NP_005227.1:p.Thr669Ala
|
|