ENST00000452508.7:c.4255C>T
|
ENSP00000388058.2:p.Leu1419Phe
|
|
ENST00000713593.1:c.*3726C>T
|
ENSP00000518889.1:n.*3726C>T
|
|
ENST00000278616.9:c.4255C>T
|
ENSP00000278616.4:p.Leu1419Phe
|
|
ENST00000533733.6:n.1518C>T
|
|
|
ENST00000683174.1:n.4405C>T
|
|
|
ENST00000527805.6:c.4255C>T
|
ENSP00000435747.2:p.Leu1419Phe
|
|
ENST00000675595.1:c.4090C>T
|
ENSP00000502563.1:p.Leu1364Phe
|
|
ENST00000675843.1:c.4255C>T
MANE Select
|
ENSP00000501606.1:p.Leu1419Phe
|
|
ENST00000278616.8:c.4255C>T
|
ENSP00000278616.4:p.Leu1419Phe
|
|
ENST00000452508.6:c.4255C>T
|
ENSP00000388058.2:p.Leu1419Phe
|
|
ENST00000524792.5:n.470C>T
|
|
|
ENST00000531525.2:c.262C>T
|
ENSP00000434327.2:p.Leu88Phe
|
|
ENST00000533733.5:n.684C>T
|
|
|
NM_000051.3:c.4255C>T , LRG_135t1:c.4255C>T
|
NP_000042.3:p.Leu1419Phe
|
|
XM_005271561.3:c.4255C>T
|
XP_005271618.2:p.Leu1419Phe
|
|
XM_005271562.3:c.4255C>T
|
XP_005271619.2:p.Leu1419Phe
|
|
XM_006718843.2:c.4255C>T
|
XP_006718906.1:p.Leu1419Phe
|
|
XM_006718845.1:c.211C>T
|
XP_006718908.1:p.Leu71Phe
|
|
XM_011542840.1:c.4255C>T
|
XP_011541142.1:p.Leu1419Phe
|
|
XM_011542841.1:c.4255C>T
|
XP_011541143.1:p.Leu1419Phe
|
|
XM_011542842.1:c.4090C>T
|
XP_011541144.1:p.Leu1364Phe
|
|
XM_011542843.1:c.4255C>T
|
XP_011541145.1:p.Leu1419Phe
|
|
XM_011542844.1:c.3211C>T
|
XP_011541146.1:p.Leu1071Phe
|
|
XM_011542845.1:c.2947C>T
|
XP_011541147.1:p.Leu983Phe
|
|
XM_011542846.1:c.4255C>T
|
XP_011541148.1:p.Leu1419Phe
|
|
NM_001351834.1:c.4255C>T
|
NP_001338763.1:p.Leu1419Phe
|
|
XM_005271562.5:c.4255C>T
|
XP_005271619.2:p.Leu1419Phe
|
|
XM_006718843.4:c.4255C>T
|
XP_006718906.1:p.Leu1419Phe
|
|
XM_006718845.2:c.211C>T
|
XP_006718908.1:p.Leu71Phe
|
|
XM_011542840.3:c.4255C>T
|
XP_011541142.1:p.Leu1419Phe
|
|
XM_011542842.3:c.4090C>T
|
XP_011541144.1:p.Leu1364Phe
|
|
XM_011542843.2:c.4255C>T
|
XP_011541145.1:p.Leu1419Phe
|
|
XM_011542844.3:c.3211C>T
|
XP_011541146.1:p.Leu1071Phe
|
|
XM_011542845.2:c.2947C>T
|
XP_011541147.1:p.Leu983Phe
|
|
XM_017017789.2:c.4255C>T
|
XP_016873278.1:p.Leu1419Phe
|
|
XM_017017790.2:c.4255C>T
|
XP_016873279.1:p.Leu1419Phe
|
|
XM_017017791.1:c.4255C>T
|
XP_016873280.1:p.Leu1419Phe
|
|
XM_017017792.2:c.4255C>T
|
XP_016873281.1:p.Leu1419Phe
|
|
XR_002957150.1:n.4988C>T
|
|
|
NM_001351834.2:c.4255C>T
|
NP_001338763.1:p.Leu1419Phe
|
|
NM_000051.4:c.4255C>T
MANE Select
|
NP_000042.3:p.Leu1419Phe
|
|