ENST00000703986.1:c.7477C>T
|
ENSP00000515603.1:p.His2493Tyr
|
|
ENST00000703987.1:c.7525C>T
|
ENSP00000515604.1:p.His2509Tyr
|
|
ENST00000704649.1:c.3685-1856C>T
|
ENSP00000515974.1:n.3685-1856C>T
|
|
ENST00000704650.1:c.7462C>T
|
ENSP00000515975.1:p.His2488Tyr
|
|
ENST00000704651.1:c.7309C>T
|
ENSP00000515976.1:p.His2437Tyr
|
|
ENST00000704652.1:c.6561C>T
|
|
|
ENST00000704654.1:c.4341C>T
|
|
|
ENST00000704655.1:c.3605C>T
|
ENSP00000515980.1:n.3605C>T
|
|
ENST00000704656.1:c.2913C>T
|
ENSP00000515981.1:n.2913C>T
|
|
ENST00000324545.9:c.7510C>T
|
ENSP00000316357.6:p.His2504Tyr
|
|
ENST00000378308.7:c.7462C>T
MANE Select
|
ENSP00000367558.2:p.His2488Tyr
|
|
ENST00000324545.8:c.7510C>T
|
ENSP00000316357.6:p.His2504Tyr
|
|
ENST00000378308.6:c.7462C>T
|
ENSP00000367558.2:p.His2488Tyr
|
|
NM_001039590.2:c.7510C>T
|
NP_001034679.2:p.His2504Tyr
|
|
NM_001039591.2:c.7462C>T
|
NP_001034680.2:p.His2488Tyr
|
|
XM_005272675.3:c.7525C>T
|
XP_005272732.1:p.His2509Tyr
|
|
XM_005272676.3:c.7477C>T
|
XP_005272733.1:p.His2493Tyr
|
|
XM_005272675.4:c.7525C>T
|
XP_005272732.1:p.His2509Tyr
|
|
XM_005272676.4:c.7477C>T
|
XP_005272733.1:p.His2493Tyr
|
|
NM_001039591.3:c.7462C>T
MANE Select
|
NP_001034680.2:p.His2488Tyr
|
|
NM_001039590.3:c.7510C>T
|
NP_001034679.2:p.His2504Tyr
|
|