ENST00000324001.8:c.2319G>C
MANE Select
|
ENSP00000326018.6:p.Glu773Asp
|
|
ENST00000673881.1:c.1902G>C
|
ENSP00000501070.1:p.Glu634Asp
|
|
ENST00000674005.2:c.2604G>C
|
ENSP00000501261.1:p.Glu868Asp
|
|
ENST00000674773.1:c.1902G>C
|
ENSP00000502579.1:p.Glu634Asp
|
|
ENST00000675517.1:c.2194G>C
|
|
|
ENST00000676076.1:c.2180G>C
|
|
|
ENST00000676260.1:c.2281G>C
|
|
|
ENST00000676316.1:c.2206G>C
|
|
|
ENST00000291825.11:c.*2524G>C
|
ENSP00000291825.6:n.*2524G>C
|
|
ENST00000324001.7:c.2319G>C
|
ENSP00000326018.6:p.Glu773Asp
|
|
NM_020956.2:c.*2524G>C , LRG_265t1:c.*2524G>C
|
NP_066007.1:n.*2524G>C
|
|
NM_181882.2:c.2319G>C , LRG_265t2:c.2319G>C
|
NP_870998.2:p.Glu773Asp
|
|
XM_011527171.1:c.2319G>C
|
XP_011525473.1:p.Glu773Asp
|
|
XM_011527171.2:c.2319G>C
|
XP_011525473.1:p.Glu773Asp
|
|
XM_017027046.1:c.2217G>C
|
XP_016882535.1:p.Glu739Asp
|
|
XM_017027047.1:c.2217G>C
|
XP_016882536.1:p.Glu739Asp
|
|
NM_181882.3:c.2319G>C
MANE Select
|
NP_870998.2:p.Glu773Asp
|
|