ENST00000328194.8:c.2364A>C
MANE Select
|
ENSP00000328524.3:p.Glu788Asp
|
|
ENST00000530780.2:c.*2190A>C
|
ENSP00000433925.1:n.*2190A>C
|
|
ENST00000679446.1:n.2285A>C
|
|
|
ENST00000679458.1:n.3765A>C
|
|
|
ENST00000679460.1:n.2153A>C
|
|
|
ENST00000679568.1:c.2364A>C
|
ENSP00000505860.1:p.Glu788Asp
|
|
ENST00000679745.1:n.2153A>C
|
|
|
ENST00000679926.1:n.1180A>C
|
|
|
ENST00000679999.1:c.2364A>C
|
ENSP00000505198.1:p.Glu788Asp
|
|
ENST00000680252.1:c.2153A>C
|
|
|
ENST00000680294.1:c.2364A>C
|
ENSP00000506113.1:p.Glu788Asp
|
|
ENST00000680358.1:n.1663A>C
|
|
|
ENST00000680470.1:c.*230A>C
|
ENSP00000505975.1:n.*230A>C
|
|
ENST00000680554.1:c.2076A>C
|
ENSP00000505621.1:p.Glu692Asp
|
|
ENST00000680576.1:n.2153A>C
|
|
|
ENST00000680599.1:n.2281A>C
|
|
|
ENST00000680742.1:c.2364A>C
|
ENSP00000505206.1:p.Glu788Asp
|
|
ENST00000680885.1:n.2285A>C
|
|
|
ENST00000681158.1:c.2153A>C
|
|
|
ENST00000681173.1:n.2153A>C
|
|
|
ENST00000681203.1:c.2292A>C
|
ENSP00000506456.1:p.Glu764Asp
|
|
ENST00000681425.1:n.2285A>C
|
|
|
ENST00000328194.7:c.2364A>C
|
ENSP00000328524.3:p.Glu788Asp
|
|
ENST00000526707.5:c.2292A>C
|
ENSP00000436780.1:p.Glu764Asp
|
|
ENST00000527700.5:n.1926A>C
|
|
|
ENST00000530044.5:c.2364A>C
|
ENSP00000435866.1:p.Glu788Asp
|
|
NM_001243254.1:c.2364A>C
|
NP_001230183.1:p.Glu788Asp
|
|
NM_015213.3:c.2364A>C
|
NP_056028.2:p.Glu788Asp
|
|
XM_005252832.1:c.2364A>C
|
XP_005252889.1:p.Glu788Asp
|
|
XM_011519952.1:c.2364A>C
|
XP_011518254.1:p.Glu788Asp
|
|
XM_011519953.1:c.462A>C
|
XP_011518255.1:p.Glu154Asp
|
|
XR_242782.2:n.2629A>C
|
|
|
XR_930851.1:n.2629A>C
|
|
|
XR_930852.1:n.2629A>C
|
|
|
XR_930853.1:n.2478A>C
|
|
|
NM_001348749.1:c.2292A>C
|
NP_001335678.1:p.Glu764Asp
|
|
NM_001348750.1:c.2076A>C
|
NP_001335679.1:p.Glu692Asp
|
|
NR_145966.2:n.2621A>C
|
|
|
NM_015213.4:c.2364A>C
MANE Select
|
NP_056028.2:p.Glu788Asp
|
|
NM_001243254.2:c.2364A>C
|
NP_001230183.1:p.Glu788Asp
|
|
NM_001348749.2:c.2292A>C
|
NP_001335678.1:p.Glu764Asp
|
|
NM_001348750.2:c.2076A>C
|
NP_001335679.1:p.Glu692Asp
|
|