ENST00000328194.8:c.2363A>T
MANE Select
|
ENSP00000328524.3:p.Glu788Val
|
|
ENST00000530780.2:c.*2189A>T
|
ENSP00000433925.1:n.*2189A>T
|
|
ENST00000679446.1:n.2284A>T
|
|
|
ENST00000679458.1:n.3764A>T
|
|
|
ENST00000679460.1:n.2152A>T
|
|
|
ENST00000679568.1:c.2363A>T
|
ENSP00000505860.1:p.Glu788Val
|
|
ENST00000679745.1:n.2152A>T
|
|
|
ENST00000679926.1:n.1179A>T
|
|
|
ENST00000679999.1:c.2363A>T
|
ENSP00000505198.1:p.Glu788Val
|
|
ENST00000680252.1:c.2152A>T
|
|
|
ENST00000680294.1:c.2363A>T
|
ENSP00000506113.1:p.Glu788Val
|
|
ENST00000680358.1:n.1662A>T
|
|
|
ENST00000680470.1:c.*229A>T
|
ENSP00000505975.1:n.*229A>T
|
|
ENST00000680554.1:c.2075A>T
|
ENSP00000505621.1:p.Glu692Val
|
|
ENST00000680576.1:n.2152A>T
|
|
|
ENST00000680599.1:n.2280A>T
|
|
|
ENST00000680742.1:c.2363A>T
|
ENSP00000505206.1:p.Glu788Val
|
|
ENST00000680885.1:n.2284A>T
|
|
|
ENST00000681158.1:c.2152A>T
|
|
|
ENST00000681173.1:n.2152A>T
|
|
|
ENST00000681203.1:c.2291A>T
|
ENSP00000506456.1:p.Glu764Val
|
|
ENST00000681425.1:n.2284A>T
|
|
|
ENST00000328194.7:c.2363A>T
|
ENSP00000328524.3:p.Glu788Val
|
|
ENST00000526707.5:c.2291A>T
|
ENSP00000436780.1:p.Glu764Val
|
|
ENST00000527700.5:n.1925A>T
|
|
|
ENST00000530044.5:c.2363A>T
|
ENSP00000435866.1:p.Glu788Val
|
|
NM_001243254.1:c.2363A>T
|
NP_001230183.1:p.Glu788Val
|
|
NM_015213.3:c.2363A>T
|
NP_056028.2:p.Glu788Val
|
|
XM_005252832.1:c.2363A>T
|
XP_005252889.1:p.Glu788Val
|
|
XM_011519952.1:c.2363A>T
|
XP_011518254.1:p.Glu788Val
|
|
XM_011519953.1:c.461A>T
|
XP_011518255.1:p.Glu154Val
|
|
XR_242782.2:n.2628A>T
|
|
|
XR_930851.1:n.2628A>T
|
|
|
XR_930852.1:n.2628A>T
|
|
|
XR_930853.1:n.2477A>T
|
|
|
NM_001348749.1:c.2291A>T
|
NP_001335678.1:p.Glu764Val
|
|
NM_001348750.1:c.2075A>T
|
NP_001335679.1:p.Glu692Val
|
|
NR_145966.2:n.2620A>T
|
|
|
NM_015213.4:c.2363A>T
MANE Select
|
NP_056028.2:p.Glu788Val
|
|
NM_001243254.2:c.2363A>T
|
NP_001230183.1:p.Glu788Val
|
|
NM_001348749.2:c.2291A>T
|
NP_001335678.1:p.Glu764Val
|
|
NM_001348750.2:c.2075A>T
|
NP_001335679.1:p.Glu692Val
|
|