ENST00000620913.5:c.806T>C
MANE Select
|
ENSP00000481291.1:p.Phe269Ser
|
|
ENST00000440085.5:c.806T>C
|
ENSP00000402988.1:p.Phe269Ser
|
|
ENST00000441948.5:c.806T>C
|
ENSP00000407258.1:p.Phe269Ser
|
|
ENST00000494034.5:c.389T>C
|
|
|
ENST00000497336.1:n.346-3071T>C
|
|
|
ENST00000595796.5:c.806T>C
|
ENSP00000471683.1:p.Phe269Ser
|
|
ENST00000619100.4:c.653T>C
|
ENSP00000478807.1:p.Phe218Ser
|
|
ENST00000620913.4:c.806T>C
|
ENSP00000481291.1:p.Phe269Ser
|
|
ENST00000622196.4:c.404T>C
|
ENSP00000484236.1:p.Phe135Ser
|
|
NM_033518.3:c.806T>C
|
NP_277053.2:p.Phe269Ser
|
|
XM_005272694.3:c.947T>C
|
XP_005272751.2:p.Phe316Ser
|
|
XM_005272695.3:c.806T>C
|
XP_005272752.2:p.Phe269Ser
|
|
XM_005272697.2:c.824T>C
|
XP_005272754.2:p.Phe275Ser
|
|
XM_005272698.3:c.806T>C
|
XP_005272755.2:p.Phe269Ser
|
|
XM_006724569.2:c.806T>C
|
XP_006724632.1:p.Phe269Ser
|
|
XM_005272695.4:c.947T>C
|
XP_005272752.3:p.Phe316Ser
|
|
XM_005272698.5:c.806T>C
|
XP_005272755.2:p.Phe269Ser
|
|
XM_006724569.3:c.806T>C
|
XP_006724632.1:p.Phe269Ser
|
|
XM_017029960.1:c.824T>C
|
XP_016885449.1:p.Phe275Ser
|
|
XM_017029961.2:c.806T>C
|
XP_016885450.1:p.Phe269Ser
|
|
NM_033518.4:c.806T>C
MANE Select
|
NP_277053.2:p.Phe269Ser
|
|