ENST00000271588.9:c.12994A>T
MANE Select
|
ENSP00000271588.4:p.Asn4332Tyr
|
|
ENST00000271588.8:c.12994A>T
|
ENSP00000271588.4:p.Asn4332Tyr
|
|
NM_031935.2:c.12994A>T
|
NP_114141.2:p.Asn4332Tyr
|
|
XM_011510037.1:c.12709A>T
|
XP_011508339.1:p.Asn4237Tyr
|
|
XM_011510038.1:c.12994A>T
|
XP_011508340.1:p.Asn4332Tyr
|
|
XM_011510039.1:c.12994A>T
|
XP_011508341.1:p.Asn4332Tyr
|
|
XM_011510038.3:c.12994A>T
|
XP_011508340.1:p.Asn4332Tyr
|
|
XM_017002437.1:c.11017A>T
|
XP_016857926.1:p.Asn3673Tyr
|
|
NM_031935.3:c.12994A>T
MANE Select
|
NP_114141.2:p.Asn4332Tyr
|
|