|
NM_004453.4:c.1659T>G
MANE Select
|
NP_004444.2:p.Tyr553Ter
|
|
ENST00000511912.6:c.1659T>G
MANE Select
|
ENSP00000426638.1:p.Tyr553Ter
|
|
NM_001281737.1:c.1518T>G
|
NP_001268666.1:p.Tyr506Ter
|
|
NM_001281737.2:c.1518T>G
|
NP_001268666.1:p.Tyr506Ter
|
|
NM_001281738.1:c.1476T>G
|
NP_001268667.1:p.Tyr492Ter
|
|
NM_004453.3:c.1659T>G
|
NP_004444.2:p.Tyr553Ter
|
|
ENST00000307738.5:c.1518T>G
|
ENSP00000303552.5:p.Tyr506Ter
|
|
ENST00000506422.1:n.629T>G
|
|
|
ENST00000511912.5:c.1659T>G
|
ENSP00000426638.1:p.Tyr553Ter
|
|
ENST00000681978.1:n.3195T>G
|
|
|
ENST00000682178.1:n.2691T>G
|
|
|
ENST00000682345.1:c.*1359T>G
|
ENSP00000508122.1:n.*1359T>G
|
|
ENST00000682452.1:n.1990T>G
|
|
|
ENST00000682456.1:c.1518T>G
|
ENSP00000508240.1:p.Tyr506Ter
|
|
ENST00000682566.1:n.2442T>G
|
|
|
ENST00000682613.1:n.1971T>G
|
|
|
ENST00000682734.1:c.486T>G
|
ENSP00000507860.1:p.Tyr162Ter
|
|
ENST00000682820.1:n.1696T>G
|
|
|
ENST00000683004.1:c.*1352T>G
|
ENSP00000506936.1:n.*1352T>G
|
|
ENST00000683079.1:c.*1084T>G
|
ENSP00000507296.1:n.*1084T>G
|
|
ENST00000683081.1:c.*1496T>G
|
ENSP00000507722.1:n.*1496T>G
|
|
ENST00000683181.1:n.938T>G
|
|
|
ENST00000683209.1:n.3985T>G
|
|
|
ENST00000683305.1:c.1476T>G
|
ENSP00000508043.1:p.Tyr492Ter
|
|
ENST00000683448.1:c.*579T>G
|
ENSP00000506931.1:n.*579T>G
|
|
ENST00000683478.1:c.*1010T>G
|
ENSP00000507793.1:n.*1010T>G
|
|
ENST00000683483.1:c.1515T>G
|
ENSP00000507719.1:p.Tyr505Ter
|
|
ENST00000683622.1:n.1373T>G
|
|
|
ENST00000683751.1:c.1164T>G
|
ENSP00000506944.1:p.Tyr388Ter
|
|
ENST00000684036.1:c.1476T>G
|
ENSP00000507276.1:p.Tyr492Ter
|
|
ENST00000684129.1:c.486T>G
|
ENSP00000507174.1:p.Tyr162Ter
|
|
ENST00000684209.1:n.2034T>G
|
|
|
ENST00000684296.1:c.*579T>G
|
ENSP00000507740.1:n.*579T>G
|
|
ENST00000684505.1:c.1608T>G
|
ENSP00000508237.1:p.Tyr536Ter
|
|
ENST00000684552.1:c.*3078T>G
|
ENSP00000506899.1:n.*3078T>G
|
|
ENST00000684611.1:n.3387T>G
|
|
|
ENST00000684622.1:c.1659T>G
|
ENSP00000507546.1:p.Tyr553Ter
|
|
ENST00000684627.1:c.1476T>G
|
ENSP00000507471.1:p.Tyr492Ter
|
|
ENST00000684641.1:c.1374T>G
|
ENSP00000507642.1:p.Tyr458Ter
|
|
ENST00000684675.1:c.*506T>G
|
ENSP00000506934.1:n.*506T>G
|
|
ENST00000684749.1:n.1728T>G
|
|
|
XM_024453935.1:c.1476T>G
|
XP_024309703.1:p.Tyr492Ter
|
