ENST00000435817.7:c.747G>A
MANE Select
|
ENSP00000399259.2:p.Leu249=
|
|
ENST00000435817.6:c.747G>A
|
ENSP00000399259.2:p.Leu249=
|
|
ENST00000522126.5:c.519G>A
|
ENSP00000427796.1:p.Leu173=
|
|
ENST00000522386.1:n.353G>A
|
|
|
ENST00000522763.5:n.51G>A
|
|
|
ENST00000522783.5:c.741G>A
|
ENSP00000428677.1:p.Leu247=
|
|
ENST00000523856.5:n.5G>A
|
|
|
NM_033449.2:c.747G>A
|
NP_258260.1:p.Leu249=
|
|
XM_005268524.3:c.741G>A
|
XP_005268581.1:p.Leu247=
|
|
XM_006714803.2:c.618G>A
|
XP_006714866.1:p.Leu206=
|
|
XM_011537698.1:c.747G>A
|
XP_011536000.1:p.Leu249=
|
|
XM_011537699.1:c.747G>A
|
XP_011536001.1:p.Leu249=
|
|
XM_011537700.1:c.747G>A
|
XP_011536002.1:p.Leu249=
|
|
XM_011537701.1:c.747G>A
|
XP_011536003.1:p.Leu249=
|
|
XR_427781.2:n.801G>A
|
|
|
XR_944338.1:n.807G>A
|
|
|
XR_944339.1:n.807G>A
|
|
|
XM_005268524.5:c.741G>A
|
XP_005268581.1:p.Leu247=
|
|
XM_006714803.4:c.618G>A
|
XP_006714866.1:p.Leu206=
|
|
XM_011537698.3:c.747G>A
|
XP_011536000.1:p.Leu249=
|
|
XM_011537700.3:c.747G>A
|
XP_011536002.1:p.Leu249=
|
|
XM_011537701.3:c.747G>A
|
XP_011536003.1:p.Leu249=
|
|
XM_017010013.2:c.747G>A
|
XP_016865502.1:p.Leu249=
|
|
XR_002956197.1:n.743G>A
|
|
|
XR_427781.4:n.743G>A
|
|
|
XR_944338.3:n.822G>A
|
|
|
XR_944339.3:n.822G>A
|
|
|
NM_033449.3:c.747G>A
MANE Select
|
NP_258260.1:p.Leu249=
|
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