ENST00000275300.3:c.1259C>T
MANE Select
|
ENSP00000275300.2:p.Ala420Val
|
|
ENST00000275300.2:c.1259C>T
|
ENSP00000275300.2:p.Ala420Val
|
|
NM_021977.3:c.1259C>T
|
NP_068812.1:p.Ala420Val
|
|
XM_005267106.3:c.866C>T
|
XP_005267163.1:p.Ala289Val
|
|
XM_011536075.1:c.803C>T
|
XP_011534377.1:p.Ala268Val
|
|
XM_011536076.1:c.803C>T
|
XP_011534378.1:p.Ala268Val
|
|
XM_011536077.1:c.803C>T
|
XP_011534379.1:p.Ala268Val
|
|
XR_245546.1:n.1018-5579C>T
|
|
|
XM_005267106.5:c.866C>T
|
XP_005267163.1:p.Ala289Val
|
|
XM_011536075.2:c.803C>T
|
XP_011534377.1:p.Ala268Val
|
|
XM_011536076.3:c.803C>T
|
XP_011534378.1:p.Ala268Val
|
|
XM_017011203.2:c.803C>T
|
XP_016866692.1:p.Ala268Val
|
|
XR_001743588.1:n.1203C>T
|
|
|
XR_001743589.1:n.1018-5579C>T
|
|
|
NM_021977.4:c.1259C>T
MANE Select
|
NP_068812.1:p.Ala420Val
|
|