ENST00000379942.5:c.1604A>G
MANE Select
|
ENSP00000369274.4:p.Asp535Gly
|
|
ENST00000379942.4:c.1604A>G
|
ENSP00000369274.4:p.Asp535Gly
|
|
ENST00000464455.1:n.173A>G
|
|
|
NM_000292.2:c.1604A>G
|
NP_000283.1:p.Asp535Gly
|
|
XM_005274548.3:c.1604A>G
|
XP_005274605.1:p.Asp535Gly
|
|
XM_005274550.3:c.1604A>G
|
XP_005274607.1:p.Asp535Gly
|
|
XM_006724496.2:c.1604A>G
|
XP_006724559.1:p.Asp535Gly
|
|
XM_006724498.2:c.1058A>G
|
XP_006724561.1:p.Asp353Gly
|
|
XM_011545537.1:c.1505A>G
|
XP_011543839.1:p.Asp502Gly
|
|
XM_011545538.1:c.587A>G
|
XP_011543840.1:p.Asp196Gly
|
|
XR_950461.1:n.1788A>G
|
|
|
XM_005274548.5:c.1604A>G
|
XP_005274605.1:p.Asp535Gly
|
|
XM_005274550.5:c.1604A>G
|
XP_005274607.1:p.Asp535Gly
|
|
XM_006724496.4:c.1604A>G
|
XP_006724559.1:p.Asp535Gly
|
|
XM_006724498.4:c.1058A>G
|
XP_006724561.1:p.Asp353Gly
|
|
XM_011545537.3:c.1505A>G
|
XP_011543839.1:p.Asp502Gly
|
|
XM_011545538.3:c.587A>G
|
XP_011543840.1:p.Asp196Gly
|
|
XM_017029580.2:c.698A>G
|
XP_016885069.1:p.Asp233Gly
|
|
XR_001755697.2:n.1774A>G
|
|
|
XR_001755698.2:n.1774A>G
|
|
|
XR_002958777.1:n.1774A>G
|
|
|
XR_950461.3:n.1774A>G
|
|
|
NM_000292.3:c.1604A>G
MANE Select
|
NP_000283.1:p.Asp535Gly
|
|