ENST00000409110.6:c.1131A>T
MANE Select
|
ENSP00000386444.1:p.Leu377Phe
|
|
ENST00000409110.5:c.1131A>T
|
ENSP00000386444.1:p.Leu377Phe
|
|
ENST00000412969.6:n.2351A>T
|
|
|
ENST00000471884.5:n.3162A>T
|
|
|
ENST00000474220.5:n.337A>T
|
|
|
ENST00000476500.5:n.6430A>T
|
|
|
ENST00000492629.1:n.92A>T
|
|
|
NM_000541.4:c.1131A>T
|
NP_000532.2:p.Leu377Phe
|
|
XM_011511589.1:c.1131A>T
|
XP_011509891.1:p.Leu377Phe
|
|
XM_011511590.1:c.1131A>T
|
XP_011509892.1:p.Leu377Phe
|
|
XM_011511591.1:c.1121A>T
|
XP_011509893.1:p.Ter374Leu
|
|
XM_011511592.1:c.975A>T
|
XP_011509894.1:p.Leu325Phe
|
|
XM_011511593.1:c.831A>T
|
XP_011509895.1:p.Leu277Phe
|
|
XM_011511594.1:c.759A>T
|
XP_011509896.1:p.Leu253Phe
|
|
XM_011511596.1:c.729A>T
|
XP_011509898.1:p.Leu243Phe
|
|
XM_011511597.1:c.729A>T
|
XP_011509899.1:p.Leu243Phe
|
|
XR_922978.1:n.1448A>T
|
|
|
XR_922979.1:n.1452A>T
|
|
|
XR_922980.1:n.1547A>T
|
|
|
XM_011511593.3:c.831A>T
|
XP_011509895.1:p.Leu277Phe
|
|
XM_017004641.1:c.1121A>T
|
XP_016860130.1:p.Ter374Leu
|
|
XM_024453036.1:c.719A>T
|
XP_024308804.1:p.Ter240Leu
|
|
XR_001738882.1:n.1329A>T
|
|
|
XR_922980.2:n.1547A>T
|
|
|
NM_000541.5:c.1131A>T
MANE Select
|
NP_000532.2:p.Leu377Phe
|
|