ENST00000257215.10:c.1005C>T
MANE Select
|
ENSP00000257215.5:p.Phe335=
|
|
ENST00000257215.9:c.1005C>T
|
ENSP00000257215.5:p.Phe335=
|
|
ENST00000540717.1:c.*478C>T
|
ENSP00000440264.1:n.*478C>T
|
|
NM_006133.2:c.1005C>T
|
NP_006124.1:p.Phe335=
|
|
XM_005274230.3:c.1005C>T
|
XP_005274287.1:p.Phe335=
|
|
XM_011545235.1:c.1005C>T
|
XP_011543537.1:p.Phe335=
|
|
XM_011545236.1:c.1005C>T
|
XP_011543538.1:p.Phe335=
|
|
XM_017018238.1:c.1083C>T
|
XP_016873727.1:p.Phe361=
|
|
XM_017018239.1:c.1083C>T
|
XP_016873728.1:p.Phe361=
|
|
XM_017018240.1:c.1083C>T
|
XP_016873729.1:p.Phe361=
|
|
NM_006133.3:c.1005C>T
MANE Select
|
NP_006124.1:p.Phe335=
|
|