|
ENST00000461280.2:n.577T>C
|
|
|
|
ENST00000684116.1:n.172T>C
|
|
|
|
ENST00000684241.1:n.2112T>C
|
|
|
|
ENST00000262186.10:c.1279T>C
MANE Select
|
ENSP00000262186.5:p.Tyr427His
|
|
|
ENST00000330883.9:c.259T>C
|
ENSP00000328531.4:p.Tyr87His
|
|
|
ENST00000262186.9:c.1279T>C
|
ENSP00000262186.5:p.Tyr427His
|
|
|
ENST00000330883.8:c.259T>C
|
ENSP00000328531.4:p.Tyr87His
|
|
|
ENST00000430723.4:c.931T>C
|
ENSP00000387657.4:p.Tyr311His
|
|
|
ENST00000461280.1:n.566T>C
|
|
|
|
ENST00000473610.5:n.584T>C
|
|
|
|
ENST00000532957.5:n.1502T>C
|
|
|
|
NM_000238.3:c.1279T>C , LRG_288t1:c.1279T>C
|
NP_000229.1:p.Tyr427His
|
|
|
NM_001204798.1:c.259T>C
|
NP_001191727.1:p.Tyr87His
|
|
|
NM_172056.2:c.1279T>C , LRG_288t2:c.1279T>C
|
NP_742053.1:p.Tyr427His
|
|
|
NM_172057.2:c.259T>C , LRG_288t3:c.259T>C
|
NP_742054.1:p.Tyr87His
|
|
|
XM_011516185.1:c.979T>C
|
XP_011514487.1:p.Tyr327His
|
|
|
XM_011516186.1:c.1279T>C
|
XP_011514488.1:p.Tyr427His
|
|
|
XM_011516185.2:c.979T>C
|
XP_011514487.1:p.Tyr327His
|
|
|
XM_011516186.3:c.1279T>C
|
XP_011514488.1:p.Tyr427His
|
|
|
XM_017012195.1:c.1129T>C
|
XP_016867684.1:p.Tyr377His
|
|
|
XM_017012196.1:c.1102T>C
|
XP_016867685.1:p.Tyr368His
|
|
|
NM_000238.4:c.1279T>C
MANE Select
|
NP_000229.1:p.Tyr427His
|
|
|
NM_001204798.2:c.259T>C
|
NP_001191727.1:p.Tyr87His
|
|
|
NM_172057.3:c.259T>C
|
NP_742054.1:p.Tyr87His
|
|
