ENST00000698508.1:c.1755C>A
|
ENSP00000513759.1:p.Asp585Glu
|
|
ENST00000698509.1:n.1895C>A
|
|
|
ENST00000264972.10:c.1755C>A
MANE Select
|
ENSP00000264972.5:p.Asp585Glu
|
|
ENST00000264972.9:c.1755C>A
|
ENSP00000264972.5:p.Asp585Glu
|
|
ENST00000451498.2:c.834C>A
|
ENSP00000400475.2:p.Asp278Glu
|
|
ENST00000463643.5:n.1616C>A
|
|
|
ENST00000487283.5:n.2807C>A
|
|
|
NM_001079.3:c.1755C>A , LRG_126t1:c.1755C>A
|
NP_001070.2:p.Asp585Glu
|
|
NM_207519.1:c.834C>A
|
NP_997402.1:p.Asp278Glu
|
|
XM_005264015.3:c.1737C>A
|
XP_005264072.1:p.Asp579Glu
|
|
XM_011511783.1:c.1736+1286C>A
|
XP_011510085.1:n.1736+1286C>A
|
|
XR_923018.1:n.1938+1286C>A
|
|
|
XR_923019.1:n.1938+1286C>A
|
|
|
XR_923020.1:n.2166C>A
|
|
|
XM_017004867.1:c.2124C>A
|
XP_016860356.1:p.Asp708Glu
|
|
XM_017004868.1:c.2106C>A
|
XP_016860357.1:p.Asp702Glu
|
|
XM_017004869.1:c.2105+1286C>A
|
XP_016860358.1:n.2105+1286C>A
|
|
XR_001738925.1:n.3344+1286C>A
|
|
|
XR_001738926.1:n.3344+1286C>A
|
|
|
XR_001738927.1:n.3572C>A
|
|
|
NM_001079.4:c.1755C>A
MANE Select
|
NP_001070.2:p.Asp585Glu
|
|
NM_001378594.1:c.1755C>A
|
NP_001365523.1:p.Asp585Glu
|
|
NM_207519.2:c.834C>A
|
NP_997402.1:p.Asp278Glu
|
|