ENST00000273064.11:c.216T>C
MANE Select
|
ENSP00000273064.6:p.Asn72=
|
|
ENST00000273064.10:c.216T>C
|
ENSP00000273064.6:p.Asn72=
|
|
ENST00000295701.9:c.216T>C
|
ENSP00000295701.5:p.Asn72=
|
|
ENST00000432877.5:c.*108T>C
|
ENSP00000392394.1:n.*108T>C
|
|
ENST00000542068.5:c.216T>C
|
ENSP00000443687.1:p.Asn72=
|
|
ENST00000627282.2:c.216T>C
|
ENSP00000486540.1:p.Asn72=
|
|
NM_001271634.1:c.216T>C
|
NP_001258563.1:p.Asn72=
|
|
NM_001271635.1:c.216T>C
|
NP_001258564.1:p.Asn72=
|
|
NM_005444.2:c.216T>C
|
NP_005435.1:p.Asn72=
|
|
NR_073390.1:n.591T>C
|
|
|
XM_011512138.1:c.57T>C
|
XP_011510440.1:p.Asn19=
|
|
XM_011512138.3:c.57T>C
|
XP_011510440.1:p.Asn19=
|
|
XM_017005248.1:c.54T>C
|
XP_016860737.1:p.Asn18=
|
|
XM_017005249.2:c.57T>C
|
XP_016860738.1:p.Asn19=
|
|
NM_001271634.2:c.216T>C
|
NP_001258563.1:p.Asn72=
|
|
NM_005444.3:c.216T>C
MANE Select
|
NP_005435.1:p.Asn72=
|
|
NR_073390.2:n.332T>C
|
|
|
NM_001271635.2:c.216T>C
|
NP_001258564.1:p.Asn72=
|
|