ENST00000553106.6:c.1188G>T
MANE Select
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ENSP00000448059.1:p.Lys396Asn
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|
ENST00000307000.7:c.1173G>T
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ENSP00000303500.2:p.Lys391Asn
|
|
ENST00000549247.6:n.947G>T
|
|
|
ENST00000551114.2:n.850G>T
|
|
|
ENST00000553106.5:c.1188G>T
|
ENSP00000448059.1:p.Lys396Asn
|
|
ENST00000635477.1:c.292G>T
|
|
|
ENST00000635528.1:n.703G>T
|
|
|
NM_000277.1:c.1188G>T
|
NP_000268.1:p.Lys396Asn
|
|
XM_011538422.1:c.1131G>T
|
XP_011536724.1:p.Lys377Asn
|
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NM_000277.2:c.1188G>T
|
NP_000268.1:p.Lys396Asn
|
|
NM_001354304.1:c.1188G>T
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NP_001341233.1:p.Lys396Asn
|
|
NM_000277.3:c.1188G>T
MANE Select
|
NP_000268.1:p.Lys396Asn
|
|
NM_001354304.2:c.1188G>T
|
NP_001341233.1:p.Lys396Asn
|
|