ENST00000261819.8:c.1668A>T
MANE Select
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ENSP00000261819.3:p.Gln556His
|
|
ENST00000261819.7:c.1668A>T
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ENSP00000261819.3:p.Gln556His
|
|
ENST00000366333.3:n.880A>T
|
|
|
ENST00000441917.6:c.1332A>T
|
ENSP00000415061.2:p.Gln444His
|
|
ENST00000534976.5:n.2324A>T
|
|
|
ENST00000535482.1:c.666A>T
|
ENSP00000438754.1:p.Gln222His
|
|
ENST00000535641.5:n.1879A>T
|
|
|
ENST00000539079.5:c.1012A>T
|
|
|
ENST00000541887.5:c.1629A>T
|
ENSP00000439875.1:p.Gln543His
|
|
ENST00000544314.5:n.786A>T
|
|
|
ENST00000545218.5:n.911A>T
|
|
|
NM_001137559.1:c.1332A>T
|
NP_001131031.1:p.Gln444His
|
|
NM_016237.4:c.1668A>T
|
NP_057321.2:p.Gln556His
|
|
XM_005253900.2:c.1629A>T
|
XP_005253957.1:p.Gln543His
|
|
XM_006719449.1:c.474A>T
|
XP_006719512.1:p.Gln158His
|
|
NM_001330489.1:c.1629A>T
|
NP_001317418.1:p.Gln543His
|
|
XM_017019423.2:c.474A>T
|
XP_016874912.1:p.Gln158His
|
|
XM_017019424.2:c.474A>T
|
XP_016874913.1:p.Gln158His
|
|
NM_016237.5:c.1668A>T
MANE Select
|
NP_057321.2:p.Gln556His
|
|
NM_001330489.2:c.1629A>T
|
NP_001317418.1:p.Gln543His
|
|