ENST00000262418.12:c.1976T>G
MANE Select
|
ENSP00000262418.6:p.Phe659Cys
|
|
ENST00000262418.10:c.1976T>G
|
ENSP00000262418.6:p.Phe659Cys
|
|
ENST00000399246.3:c.878T>G
|
ENSP00000382190.3:p.Phe293Cys
|
|
NM_000342.3:c.1976T>G
|
NP_000333.1:p.Phe659Cys
|
|
XM_005257593.3:c.1781T>G
|
XP_005257650.1:p.Phe594Cys
|
|
XM_011525129.1:c.1886T>G
|
XP_011523431.1:p.Phe629Cys
|
|
XM_011525130.1:c.1976T>G
|
XP_011523432.1:p.Phe659Cys
|
|
XM_011525131.1:c.1976T>G
|
XP_011523433.1:p.Phe659Cys
|
|
XM_005257593.5:c.1781T>G
|
XP_005257650.1:p.Phe594Cys
|
|
XM_011525129.2:c.1886T>G
|
XP_011523431.1:p.Phe629Cys
|
|
NM_000342.4:c.1976T>G
MANE Select
|
NP_000333.1:p.Phe659Cys
|
|