ENST00000356231.4:c.2127G>T
MANE Select
|
ENSP00000348564.3:p.Leu709Phe
|
|
ENST00000643434.1:c.*1305G>T
|
ENSP00000494699.1:n.*1305G>T
|
|
ENST00000356231.3:c.2127G>T
|
ENSP00000348564.3:p.Leu709Phe
|
|
ENST00000562465.5:c.120G>T
|
ENSP00000454246.1:p.Leu40Phe
|
|
NM_138477.2:c.2127G>T
|
NP_612486.2:p.Leu709Phe
|
|
XM_005254176.3:c.2130G>T
|
XP_005254233.1:p.Leu710Phe
|
|
XM_011521270.1:c.2154G>T
|
XP_011519572.1:p.Leu718Phe
|
|
XM_011521271.1:c.2151G>T
|
XP_011519573.1:p.Leu717Phe
|
|
XM_011521272.1:c.2154G>T
|
XP_011519574.1:p.Leu718Phe
|
|
XM_011521273.1:c.2154G>T
|
XP_011519575.1:p.Leu718Phe
|
|
XM_011521274.1:c.1119G>T
|
XP_011519576.1:p.Leu373Phe
|
|
XM_011521275.1:c.1371G>T
|
XP_011519577.1:p.Leu457Phe
|
|
XR_931757.1:n.2127G>T
|
|
|
NM_138477.4:c.2127G>T
MANE Select
|
NP_612486.2:p.Leu709Phe
|
|
XM_005254176.5:c.2130G>T
|
XP_005254233.1:p.Leu710Phe
|
|
XM_011521270.2:c.2154G>T
|
XP_011519572.1:p.Leu718Phe
|
|
XM_011521271.2:c.2151G>T
|
XP_011519573.1:p.Leu717Phe
|
|
XM_011521274.2:c.1119G>T
|
XP_011519576.1:p.Leu373Phe
|
|
XR_001751104.1:n.2184G>T
|
|
|
XR_001751105.1:n.2184G>T
|
|
|
XR_931757.2:n.2147G>T
|
|
|