ENST00000220616.9:c.5693T>G
MANE Select
|
ENSP00000220616.4:p.Val1898Gly
|
|
ENST00000220616.8:c.5693T>G
|
ENSP00000220616.4:p.Val1898Gly
|
|
ENST00000518058.1:c.88T>G
|
|
|
ENST00000519178.5:c.1059T>G
|
|
|
ENST00000519543.5:c.155T>G
|
ENSP00000430430.1:p.Val52Gly
|
|
ENST00000523756.5:c.2348T>G
|
|
|
NM_003235.4:c.5693T>G
|
NP_003226.4:p.Val1898Gly
|
|
XM_005251038.3:c.5501T>G
|
XP_005251095.1:p.Val1834Gly
|
|
XM_005251040.3:c.5693T>G
|
XP_005251097.1:p.Val1898Gly
|
|
XM_005251042.3:c.5693T>G
|
XP_005251099.1:p.Val1898Gly
|
|
XM_005251043.3:c.5693T>G
|
XP_005251100.1:p.Val1898Gly
|
|
XM_006716622.2:c.5693T>G
|
XP_006716685.1:p.Val1898Gly
|
|
XM_005251038.4:c.5501T>G
|
XP_005251095.1:p.Val1834Gly
|
|
XM_005251040.4:c.5693T>G
|
XP_005251097.1:p.Val1898Gly
|
|
XM_005251042.4:c.5693T>G
|
XP_005251099.1:p.Val1898Gly
|
|
XM_006716622.3:c.5693T>G
|
XP_006716685.1:p.Val1898Gly
|
|
XM_017013793.1:c.5627T>G
|
XP_016869282.1:p.Val1876Gly
|
|
XM_017013794.1:c.5693T>G
|
XP_016869283.1:p.Val1898Gly
|
|
XM_017013795.1:c.5522T>G
|
XP_016869284.1:p.Val1841Gly
|
|
XM_017013796.1:c.5474T>G
|
XP_016869285.1:p.Val1825Gly
|
|
XM_017013797.1:c.5432T>G
|
XP_016869286.1:p.Val1811Gly
|
|
XM_017013798.1:c.5693T>G
|
XP_016869287.1:p.Val1898Gly
|
|
XM_017013799.1:c.5693T>G
|
XP_016869288.1:p.Val1898Gly
|
|
XM_017013800.1:c.5693T>G
|
XP_016869289.1:p.Val1898Gly
|
|
NM_003235.5:c.5693T>G
MANE Select
|
NP_003226.4:p.Val1898Gly
|
|