ENST00000339077.10:c.1267C>T
MANE Select
|
ENSP00000343273.4:p.His423Tyr
|
|
ENST00000339077.9:c.1267C>T
|
ENSP00000343273.4:p.His423Tyr
|
|
ENST00000409689.5:c.1123C>T
|
ENSP00000386263.1:p.His375Tyr
|
|
ENST00000469576.1:n.154C>T
|
|
|
ENST00000521082.5:c.*1275C>T
|
ENSP00000430351.1:n.*1275C>T
|
|
NM_001031710.2:c.1267C>T
|
NP_001026880.2:p.His423Tyr
|
|
NM_018846.4:c.1123C>T
|
NP_061334.4:p.His375Tyr
|
|
NR_033328.1:n.1691C>T
|
|
|
XM_006715753.1:c.1306C>T
|
XP_006715816.1:p.His436Tyr
|
|
XM_006715754.1:c.1240C>T
|
XP_006715817.1:p.His414Tyr
|
|
XM_006715755.1:c.1240C>T
|
XP_006715818.1:p.His414Tyr
|
|
XM_006715756.1:c.1162C>T
|
XP_006715819.1:p.His388Tyr
|
|
XM_006715753.3:c.1306C>T
|
XP_006715816.1:p.His436Tyr
|
|
XM_006715754.3:c.1240C>T
|
XP_006715817.1:p.His414Tyr
|
|
XM_006715755.3:c.1240C>T
|
XP_006715818.1:p.His414Tyr
|
|
XM_006715756.3:c.1162C>T
|
XP_006715819.1:p.His388Tyr
|
|
XM_017012439.2:c.1201C>T
|
XP_016867928.1:p.His401Tyr
|
|
NM_001031710.3:c.1267C>T
MANE Select
|
NP_001026880.2:p.His423Tyr
|
|
NM_018846.5:c.1123C>T
|
NP_061334.4:p.His375Tyr
|
|
NR_033328.2:n.1640C>T
|
|
|