ENST00000339077.10:c.995T>G
MANE Select
|
ENSP00000343273.4:p.Val332Gly
|
|
ENST00000339077.9:c.995T>G
|
ENSP00000343273.4:p.Val332Gly
|
|
ENST00000409689.5:c.851T>G
|
ENSP00000386263.1:p.Val284Gly
|
|
ENST00000521082.5:c.*1003T>G
|
ENSP00000430351.1:n.*1003T>G
|
|
NM_001031710.2:c.995T>G
|
NP_001026880.2:p.Val332Gly
|
|
NM_018846.4:c.851T>G
|
NP_061334.4:p.Val284Gly
|
|
NR_033328.1:n.1419T>G
|
|
|
XM_006715753.1:c.1034T>G
|
XP_006715816.1:p.Val345Gly
|
|
XM_006715754.1:c.968T>G
|
XP_006715817.1:p.Val323Gly
|
|
XM_006715755.1:c.968T>G
|
XP_006715818.1:p.Val323Gly
|
|
XM_006715756.1:c.890T>G
|
XP_006715819.1:p.Val297Gly
|
|
XM_006715753.3:c.1034T>G
|
XP_006715816.1:p.Val345Gly
|
|
XM_006715754.3:c.968T>G
|
XP_006715817.1:p.Val323Gly
|
|
XM_006715755.3:c.968T>G
|
XP_006715818.1:p.Val323Gly
|
|
XM_006715756.3:c.890T>G
|
XP_006715819.1:p.Val297Gly
|
|
XM_017012439.2:c.929T>G
|
XP_016867928.1:p.Val310Gly
|
|
NM_001031710.3:c.995T>G
MANE Select
|
NP_001026880.2:p.Val332Gly
|
|
NM_018846.5:c.851T>G
|
NP_061334.4:p.Val284Gly
|
|
NR_033328.2:n.1368T>G
|
|
|