ENST00000235521.5:c.863A>C
MANE Select
|
ENSP00000235521.4:p.Glu288Ala
|
|
ENST00000235521.4:c.863A>C
|
ENSP00000235521.4:p.Glu288Ala
|
|
ENST00000369426.9:c.*229A>C
|
ENSP00000358434.5:n.*229A>C
|
|
NM_015836.3:c.863A>C
|
NP_056651.1:p.Glu288Ala
|
|
NM_201263.2:c.*229A>C
|
NP_957715.1:n.*229A>C
|
|
XM_005270350.2:c.809A>C
|
XP_005270407.1:p.Glu270Ala
|
|
XM_006710283.1:c.581A>C
|
XP_006710346.1:p.Glu194Ala
|
|
XM_011540493.1:c.794A>C
|
XP_011538795.1:p.Glu265Ala
|
|
XM_011540494.1:c.794A>C
|
XP_011538796.1:p.Glu265Ala
|
|
XM_011540495.1:c.605A>C
|
XP_011538797.1:p.Glu202Ala
|
|
XM_005270350.3:c.809A>C
|
XP_005270407.1:p.Glu270Ala
|
|
XM_011540494.2:c.794A>C
|
XP_011538796.1:p.Glu265Ala
|
|
XM_011540495.2:c.605A>C
|
XP_011538797.1:p.Glu202Ala
|
|
XM_017000038.1:c.806A>C
|
XP_016855527.1:p.Glu269Ala
|
|
XM_017000039.1:c.794A>C
|
XP_016855528.1:p.Glu265Ala
|
|
XM_017000040.1:c.692A>C
|
XP_016855529.1:p.Glu231Ala
|
|
XM_017000041.2:c.524A>C
|
XP_016855530.1:p.Glu175Ala
|
|
XM_017000042.1:c.*198A>C
|
XP_016855531.1:n.*198A>C
|
|
XM_024449826.1:c.794A>C
|
XP_024305594.1:p.Glu265Ala
|
|
XM_024449860.1:c.581A>C
|
XP_024305628.1:p.Glu194Ala
|
|
XM_024449871.1:c.581A>C
|
XP_024305639.1:p.Glu194Ala
|
|
NM_001378226.1:c.794A>C
|
NP_001365155.1:p.Glu265Ala
|
|
NM_001378227.1:c.794A>C
|
NP_001365156.1:p.Glu265Ala
|
|
NM_001378228.1:c.692A>C
|
NP_001365157.1:p.Glu231Ala
|
|
NM_001378229.1:c.605A>C
|
NP_001365158.1:p.Glu202Ala
|
|
NM_001378230.1:c.581A>C
|
NP_001365159.1:p.Glu194Ala
|
|
NM_001378231.1:c.*198A>C
|
NP_001365160.1:n.*198A>C
|
|
NM_015836.4:c.863A>C
MANE Select
|
NP_056651.1:p.Glu288Ala
|
|