ENST00000392017.9:c.881C>A
MANE Select
|
ENSP00000375872.4:p.Pro294His
|
|
ENST00000347464.9:c.392C>A
|
ENSP00000318259.6:p.Pro131His
|
|
ENST00000373525.9:c.449C>A
|
ENSP00000362625.5:p.Pro150His
|
|
ENST00000392017.8:c.881C>A
|
ENSP00000375872.4:p.Pro294His
|
|
ENST00000392018.1:c.932C>A
|
ENSP00000375873.1:p.Pro311His
|
|
ENST00000392020.8:c.824C>A
|
ENSP00000375875.4:p.Pro275His
|
|
ENST00000392021.7:c.*762C>A
|
ENSP00000375876.3:n.*762C>A
|
|
ENST00000419681.5:c.392C>A
|
ENSP00000398773.1:p.Pro131His
|
|
ENST00000444735.5:c.500C>A
|
ENSP00000409215.1:p.Pro167His
|
|
ENST00000474148.5:n.1676C>A
|
|
|
ENST00000479942.5:n.1027C>A
|
|
|
ENST00000492298.5:n.402C>A
|
|
|
ENST00000498620.5:n.388C>A
|
|
|
NM_001190266.1:c.629C>A
|
NP_001177195.1:p.Pro210His
|
|
NM_001190267.1:c.533C>A
|
NP_001177196.1:p.Pro178His
|
|
NM_017974.3:c.824C>A
|
NP_060444.3:p.Pro275His
|
|
NM_030803.6:c.881C>A
|
NP_110430.5:p.Pro294His
|
|
NM_198890.2:c.392C>A
|
NP_942593.2:p.Pro131His
|
|
XM_005246082.1:c.932C>A
|
XP_005246139.1:p.Pro311His
|
|
XM_005246084.1:c.500C>A
|
XP_005246141.1:p.Pro167His
|
|
XM_005246086.1:c.449C>A
|
XP_005246143.1:p.Pro150His
|
|
XM_006712608.1:c.680C>A
|
XP_006712671.1:p.Pro227His
|
|
XR_241242.1:n.1126C>A
|
|
|
NM_001363742.1:c.932C>A
|
NP_001350671.1:p.Pro311His
|
|
XM_005246084.2:c.500C>A
|
XP_005246141.1:p.Pro167His
|
|
XM_005246086.2:c.449C>A
|
XP_005246143.1:p.Pro150His
|
|
XM_006712608.3:c.680C>A
|
XP_006712671.1:p.Pro227His
|
|
XR_001738801.2:n.1062C>A
|
|
|
XR_241242.3:n.1113C>A
|
|
|
NM_030803.7:c.881C>A
MANE Select
|
NP_110430.5:p.Pro294His
|
|
NM_001190266.2:c.629C>A
|
NP_001177195.1:p.Pro210His
|
|
NM_001190267.2:c.533C>A
|
NP_001177196.1:p.Pro178His
|
|
NM_001363742.2:c.932C>A
|
NP_001350671.1:p.Pro311His
|
|
NM_017974.4:c.824C>A
|
NP_060444.3:p.Pro275His
|
|
NM_198890.3:c.392C>A
|
NP_942593.2:p.Pro131His
|
|