ENST00000695754.1:c.403G>C
|
ENSP00000512147.1:p.Asp135His
|
|
ENST00000695755.1:c.403G>C
|
ENSP00000512148.1:p.Asp135His
|
|
ENST00000695756.1:c.403G>C
|
ENSP00000512149.1:p.Asp135His
|
|
ENST00000695757.1:c.403G>C
|
ENSP00000512150.1:p.Asp135His
|
|
ENST00000695758.1:c.429G>C
|
ENSP00000512151.1:p.Gly143=
|
|
ENST00000695759.1:c.510G>C
|
ENSP00000512152.1:p.Gly170=
|
|
ENST00000695760.1:c.481G>C
|
ENSP00000512153.1:p.Asp161His
|
|
ENST00000695761.1:c.468G>C
|
ENSP00000512154.1:p.Gly156=
|
|
ENST00000695762.1:c.394G>C
|
ENSP00000512155.1:p.Asp132His
|
|
ENST00000695763.1:c.*572G>C
|
ENSP00000512156.1:n.*572G>C
|
|
ENST00000509305.6:c.403G>C
MANE Select
|
ENSP00000423689.1:p.Asp135His
|
|
ENST00000314933.6:c.409G>C
|
ENSP00000313967.6:p.Asp137His
|
|
ENST00000432749.6:c.403G>C
|
ENSP00000404606.2:p.Asp135His
|
|
ENST00000509305.5:c.403G>C
|
ENSP00000423689.1:p.Asp135His
|
|
ENST00000510260.5:c.403G>C
|
ENSP00000426317.1:p.Asp135His
|
|
NM_000491.3:c.409G>C , LRG_23t1:c.409G>C
|
NP_000482.3:p.Asp137His
|
|
XM_011542059.1:c.409G>C
|
XP_011540361.1:p.Asp137His
|
|
NM_000491.4:c.409G>C
|
NP_000482.3:p.Asp137His
|
|
XM_011542059.2:c.409G>C
|
XP_011540361.1:p.Asp137His
|
|
NM_000491.5:c.409G>C
|
NP_000482.3:p.Asp137His
|
|
NM_001371184.1:c.409G>C
|
NP_001358113.1:p.Asp137His
|
|
NM_001371184.3:c.403G>C
|
NP_001358113.2:p.Asp135His
|
|
NM_001378156.1:c.403G>C
MANE Select
|
NP_001365085.1:p.Asp135His
|
|