ENST00000354181.8:c.319G>T
MANE Select
|
ENSP00000346112.3:p.Asp107Tyr
|
|
ENST00000675289.1:n.1101G>T
|
|
|
ENST00000676379.1:c.319G>T
|
ENSP00000502539.1:p.Asp107Tyr
|
|
ENST00000290209.9:c.166G>T
|
ENSP00000290209.5:p.Asp56Tyr
|
|
ENST00000354181.7:c.319G>T
|
ENSP00000346112.3:p.Asp107Tyr
|
|
ENST00000397702.6:c.142G>T
|
ENSP00000380814.2:p.Asp48Tyr
|
|
ENST00000397707.6:c.274G>T
|
ENSP00000380819.2:p.Asp92Tyr
|
|
ENST00000458406.6:c.142G>T
|
ENSP00000387725.2:p.Asp48Tyr
|
|
ENST00000558589.5:c.292G>T
|
ENSP00000452776.1:p.Asp98Tyr
|
|
ENST00000558667.5:c.319G>T
|
ENSP00000453473.1:p.Asp107Tyr
|
|
ENST00000559236.5:c.319G>T
|
ENSP00000452828.1:p.Asp107Tyr
|
|
ENST00000559484.1:c.142G>T
|
ENSP00000452857.1:p.Asp48Tyr
|
|
ENST00000559523.5:c.142G>T
|
ENSP00000452904.1:p.Asp48Tyr
|
|
ENST00000559664.5:c.319G>T
|
ENSP00000453702.1:p.Asp107Tyr
|
|
ENST00000560164.5:c.-99G>T
|
ENSP00000452705.1:n.-99G>T
|
|
ENST00000560332.1:c.-99G>T
|
ENSP00000454037.1:n.-99G>T
|
|
ENST00000560611.5:c.319G>T
|
ENSP00000454168.1:p.Asp107Tyr
|
|
ENST00000561080.5:c.319G>T
|
ENSP00000454069.1:p.Asp107Tyr
|
|
ENST00000561120.5:c.292G>T
|
ENSP00000452771.1:p.Asp98Tyr
|
|
NM_001042494.1:c.142G>T
|
NP_001035959.1:p.Asp48Tyr
|
|
NM_001042495.1:c.142G>T
|
NP_001035960.1:p.Asp48Tyr
|
|
NM_001042496.1:c.292G>T
|
NP_001035961.1:p.Asp98Tyr
|
|
NM_001042497.1:c.274G>T
|
NP_001035962.1:p.Asp92Tyr
|
|
NM_005135.2:c.166G>T , LRG_270t1:c.166G>T
|
NP_005126.1:p.Asp56Tyr
|
|
NM_133647.1:c.319G>T , LRG_270t2:c.319G>T
|
NP_598408.1:p.Asp107Tyr
|
|
XM_006720793.2:c.319G>T
|
XP_006720856.1:p.Asp107Tyr
|
|
XM_011522267.1:c.319G>T
|
XP_011520569.1:p.Asp107Tyr
|
|
XM_011522268.1:c.319G>T
|
XP_011520570.1:p.Asp107Tyr
|
|
XM_011522269.1:c.319G>T
|
XP_011520571.1:p.Asp107Tyr
|
|
XR_429476.2:n.325G>T
|
|
|
XR_931960.1:n.325G>T
|
|
|
XR_931961.1:n.325G>T
|
|
|
NM_001365088.1:c.319G>T
MANE Select
|
NP_001352017.1:p.Asp107Tyr
|
|
XM_006720793.4:c.319G>T
|
XP_006720856.1:p.Asp107Tyr
|
|
XM_011522269.3:c.319G>T
|
XP_011520571.1:p.Asp107Tyr
|
|
XR_931960.3:n.1569G>T
|
|
|
NM_001042494.2:c.142G>T
|
NP_001035959.1:p.Asp48Tyr
|
|
NM_001042495.2:c.142G>T
|
NP_001035960.1:p.Asp48Tyr
|
|
NM_001042496.2:c.292G>T
|
NP_001035961.1:p.Asp98Tyr
|
|
NM_001042497.2:c.274G>T
|
NP_001035962.1:p.Asp92Tyr
|
|
NM_133647.2:c.319G>T
|
NP_598408.1:p.Asp107Tyr
|
|