ENST00000339113.9:c.1657C>T
|
|
|
ENST00000378756.8:c.1693C>T
MANE Select
|
ENSP00000368031.3:p.His565Tyr
|
|
ENST00000400830.4:c.692C>T
|
|
|
ENST00000536055.6:c.1456C>T
|
ENSP00000439290.1:p.His486Tyr
|
|
ENST00000672388.1:n.2030C>T
|
|
|
ENST00000339113.8:c.1649C>T
|
|
|
ENST00000378755.9:c.1837C>T
|
ENSP00000368030.5:p.His613Tyr
|
|
ENST00000378756.7:c.1693C>T
|
ENSP00000368031.3:p.His565Tyr
|
|
ENST00000536055.5:c.1456C>T
|
ENSP00000439290.1:p.His486Tyr
|
|
NM_001170535.1:c.1693C>T
|
NP_001164006.1:p.His565Tyr
|
|
NM_001170536.1:c.1456C>T
|
NP_001164007.1:p.His486Tyr
|
|
NM_018188.3:c.1837C>T
|
NP_060658.3:p.His613Tyr
|
|
NM_001170535.2:c.1693C>T
|
NP_001164006.1:p.His565Tyr
|
|
NM_001170536.2:c.1456C>T
|
NP_001164007.1:p.His486Tyr
|
|
NM_018188.4:c.1837C>T
|
NP_060658.3:p.His613Tyr
|
|
XM_024448098.1:c.1771C>T
|
XP_024303866.1:p.His591Tyr
|
|
XR_001737282.1:n.1766C>T
|
|
|
XR_002956997.1:n.1844C>T
|
|
|
NM_001170535.3:c.1693C>T
MANE Select
|
NP_001164006.1:p.His565Tyr
|
|
NM_018188.5:c.1837C>T
|
NP_060658.3:p.His613Tyr
|
|
NM_001170536.3:c.1456C>T
|
NP_001164007.1:p.His486Tyr
|
|