ENST00000378154.3:c.2386G>T
|
ENSP00000367396.2:p.Asp796Tyr
|
|
ENST00000378158.6:c.2383G>T
|
ENSP00000367400.2:p.Asp795Tyr
|
|
ENST00000378163.7:c.2437G>T
MANE Select
|
ENSP00000367405.1:p.Asp813Tyr
|
|
ENST00000378166.9:c.2335G>T
|
ENSP00000367408.5:p.Asp779Tyr
|
|
ENST00000378168.8:c.2440G>T
|
ENSP00000367410.4:p.Asp814Tyr
|
|
ENST00000378179.9:c.1057G>T
|
ENSP00000367421.4:p.Asp353Tyr
|
|
ENST00000421587.8:c.2368G>T
|
ENSP00000400526.4:p.Asp790Tyr
|
|
ENST00000442742.7:c.2299G>T
|
ENSP00000398007.3:p.Asp767Tyr
|
|
ENST00000642499.1:n.1216G>T
|
|
|
ENST00000643733.1:c.209G>T
|
|
|
ENST00000644219.1:c.2419G>T
|
ENSP00000495357.1:p.Asp807Tyr
|
|
ENST00000644347.1:c.2350G>T
|
ENSP00000494183.1:p.Asp784Tyr
|
|
ENST00000645566.1:c.2422G>T
|
ENSP00000494788.1:p.Asp808Tyr
|
|
ENST00000645937.2:n.2668G>T
|
|
|
ENST00000645986.2:c.2404G>T
|
ENSP00000494409.2:p.Asp802Tyr
|
|
ENST00000646087.2:c.1759G>T
|
ENSP00000495510.2:p.Asp587Tyr
|
|
ENST00000646120.2:c.2353G>T
|
ENSP00000495291.2:p.Asp785Tyr
|
|
ENST00000675354.1:c.2371G>T
|
ENSP00000502315.1:p.Asp791Tyr
|
|
ENST00000378158.5:c.2386G>T
|
ENSP00000367400.1:p.Asp796Tyr
|
|
ENST00000378163.5:c.2437G>T
|
ENSP00000367405.1:p.Asp813Tyr
|
|
ENST00000378166.8:c.2422G>T
|
ENSP00000367408.4:p.Asp808Tyr
|
|
ENST00000378168.6:c.802G>T
|
ENSP00000367410.2:p.Asp268Tyr
|
|
ENST00000378179.7:c.1213G>T
|
ENSP00000367421.3:p.Asp405Tyr
|
|
ENST00000421587.6:c.2350G>T
|
ENSP00000400526.2:p.Asp784Tyr
|
|
ENST00000442742.6:c.2353G>T
|
ENSP00000398007.2:p.Asp785Tyr
|
|
NM_001126054.2:c.2353G>T
|
NP_001119526.1:p.Asp785Tyr
|
|
NM_001126055.2:c.2350G>T
|
NP_001119527.1:p.Asp784Tyr
|
|
NM_003688.3:c.2422G>T
|
NP_003679.2:p.Asp808Tyr
|
|
XM_005272686.3:c.2419G>T
|
XP_005272743.1:p.Asp807Tyr
|
|
XM_006724566.2:c.2314G>T
|
XP_006724629.1:p.Asp772Tyr
|
|
XM_011543993.1:c.2437G>T
|
XP_011542295.1:p.Asp813Tyr
|
|
XM_011543994.1:c.2401G>T
|
XP_011542296.1:p.Asp801Tyr
|
|
XM_011543995.1:c.2368G>T
|
XP_011542297.1:p.Asp790Tyr
|
|
XM_011543996.1:c.2332G>T
|
XP_011542298.1:p.Asp778Tyr
|
|
XM_011543997.1:c.1864G>T
|
XP_011542299.1:p.Asp622Tyr
|
|
XM_005272686.4:c.2419G>T
|
XP_005272743.1:p.Asp807Tyr
|
|
XM_006724566.3:c.2314G>T
|
XP_006724629.1:p.Asp772Tyr
|
|
XM_011543993.2:c.2437G>T
|
XP_011542295.1:p.Asp813Tyr
|
|
XM_011543994.2:c.2401G>T
|
XP_011542296.1:p.Asp801Tyr
|
|
XM_011543995.2:c.2368G>T
|
XP_011542297.1:p.Asp790Tyr
|
|
XM_011543996.2:c.2332G>T
|
XP_011542298.1:p.Asp778Tyr
|
|
XM_011543997.3:c.1864G>T
|
XP_011542299.1:p.Asp622Tyr
|
|
XM_024452473.1:c.1759G>T
|
XP_024308241.1:p.Asp587Tyr
|
|
NM_001367721.1:c.2437G>T
MANE Select
|
NP_001354650.1:p.Asp813Tyr
|
|