ENST00000400521.7:c.1161A>C
MANE Select
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ENSP00000383365.1:p.Ser387=
|
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ENST00000400518.5:c.1071A>C
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ENSP00000383362.1:p.Ser357=
|
|
ENST00000400519.6:c.1158A>C
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ENSP00000383363.1:p.Ser386=
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ENST00000400521.6:c.1161A>C
|
ENSP00000383365.1:p.Ser387=
|
|
ENST00000400525.6:c.1092A>C
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ENSP00000383369.3:p.Ser364=
|
|
ENST00000462330.5:c.84A>C
|
ENSP00000485603.2:p.Ser28=
|
|
ENST00000462843.2:c.111A>C
|
ENSP00000485466.2:p.Ser37=
|
|
ENST00000474308.5:c.1104A>C
|
ENSP00000485665.1:p.Ser368=
|
|
ENST00000485358.5:c.129A>C
|
ENSP00000485499.2:p.Ser43=
|
|
ENST00000487165.5:n.1255A>C
|
|
|
ENST00000494454.5:n.1235A>C
|
|
|
ENST00000495655.2:n.705A>C
|
|
|
ENST00000542719.6:c.873A>C
|
ENSP00000485128.2:p.Ser291=
|
|
ENST00000634471.1:n.244-372A>C
|
|
|
ENST00000634537.1:c.390A>C
|
ENSP00000489208.1:p.Ser130=
|
|
NM_006440.4:c.1161A>C
|
NP_006431.2:p.Ser387=
|
|
NM_001352300.1:c.1158A>C
|
NP_001339229.1:p.Ser386=
|
|
NM_001352301.1:c.1071A>C
|
NP_001339230.1:p.Ser357=
|
|
NM_001352302.1:c.873A>C
|
NP_001339231.1:p.Ser291=
|
|
NR_147957.1:n.1293A>C
|
|
|
NM_006440.5:c.1161A>C
MANE Select
|
NP_006431.2:p.Ser387=
|
|
NM_001352300.2:c.1158A>C
|
NP_001339229.1:p.Ser386=
|
|
NR_147957.2:n.1119A>C
|
|
|
NM_001352301.2:c.1071A>C
|
NP_001339230.1:p.Ser357=
|
|
NM_001352302.2:c.873A>C
|
NP_001339231.1:p.Ser291=
|
|