ENST00000261819.8:c.1698A>G
MANE Select
|
ENSP00000261819.3:p.Lys566=
|
|
ENST00000261819.7:c.1698A>G
|
ENSP00000261819.3:p.Lys566=
|
|
ENST00000366333.3:n.910A>G
|
|
|
ENST00000441917.6:c.1362A>G
|
ENSP00000415061.2:p.Lys454=
|
|
ENST00000534976.5:n.2354A>G
|
|
|
ENST00000535482.1:c.696A>G
|
ENSP00000438754.1:p.Lys232=
|
|
ENST00000535641.5:n.1909A>G
|
|
|
ENST00000539079.5:c.1042A>G
|
|
|
ENST00000541887.5:c.1659A>G
|
ENSP00000439875.1:p.Lys553=
|
|
ENST00000544314.5:n.816A>G
|
|
|
ENST00000545218.5:n.941A>G
|
|
|
NM_001137559.1:c.1362A>G
|
NP_001131031.1:p.Lys454=
|
|
NM_016237.4:c.1698A>G
|
NP_057321.2:p.Lys566=
|
|
XM_005253900.2:c.1659A>G
|
XP_005253957.1:p.Lys553=
|
|
XM_006719449.1:c.504A>G
|
XP_006719512.1:p.Lys168=
|
|
NM_001330489.1:c.1659A>G
|
NP_001317418.1:p.Lys553=
|
|
XM_017019423.2:c.504A>G
|
XP_016874912.1:p.Lys168=
|
|
XM_017019424.2:c.504A>G
|
XP_016874913.1:p.Lys168=
|
|
NM_016237.5:c.1698A>G
MANE Select
|
NP_057321.2:p.Lys566=
|
|
NM_001330489.2:c.1659A>G
|
NP_001317418.1:p.Lys553=
|
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