ENST00000422447.8:c.892A=
MANE Select
|
ENSP00000395337.3:p.Asn298=
|
|
ENST00000227157.8:c.*42A=
|
ENSP00000227157.4:n.*42A=
|
|
ENST00000375710.7:n.1759A=
|
|
|
ENST00000379412.9:c.892A=
|
ENSP00000368722.5:p.Asn298=
|
|
ENST00000396222.6:c.688-65A=
|
ENSP00000379524.2:n.688-65A=
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|
ENST00000422447.7:c.892A=
|
ENSP00000395337.3:p.Asn298=
|
|
ENST00000430553.6:c.718A=
|
ENSP00000406172.2:p.Asn240=
|
|
ENST00000538451.1:n.779A=
|
|
|
ENST00000540430.5:c.979A=
|
ENSP00000445175.1:p.Asn327=
|
|
ENST00000542179.1:c.892A=
|
ENSP00000445331.1:p.Asn298=
|
|
ENST00000545215.5:c.*636A=
|
ENSP00000442637.1:n.*636A=
|
|
NM_001135239.1:c.718A=
|
NP_001128711.1:p.Asn240=
|
|
NM_001165414.1:c.979A=
|
NP_001158886.1:p.Asn327=
|
|
NM_001165415.1:c.688-65A=
|
NP_001158887.1:n.688-65A=
|
|
NM_001165416.1:c.*42A=
|
NP_001158888.1:n.*42A=
|
|
NM_005566.3:c.892A=
|
NP_005557.1:p.Asn298=
|
|
NR_028500.1:n.1046A=
|
|
|
NM_005566.4:c.892A=
MANE Select
|
NP_005557.1:p.Asn298=
|
|
NM_001165415.2:c.688-65A=
|
NP_001158887.1:n.688-65A=
|
|
NM_001135239.2:c.718A=
|
NP_001128711.1:p.Asn240=
|
|
NM_001165414.2:c.979A=
|
NP_001158886.1:p.Asn327=
|
|
NM_001165416.2:c.*42A=
|
NP_001158888.1:n.*42A=
|
|
NR_028500.2:n.872A=
|
|
|