|
ENST00000362021.9:c.1072G>T
MANE Select
|
ENSP00000354689.4:p.Ala358Ser
|
|
|
ENST00000354884.8:c.1051G>T
|
ENSP00000346956.4:p.Ala351Ser
|
|
|
ENST00000362021.8:c.1072G>T
|
ENSP00000354689.4:p.Ala358Ser
|
|
|
ENST00000524886.1:n.330G>T
|
|
|
|
ENST00000524928.1:c.*1402G>T
|
ENSP00000437186.1:n.*1402G>T
|
|
|
ENST00000527829.1:n.432G>T
|
|
|
|
ENST00000533076.5:c.*69G>T
|
ENSP00000434290.1:n.*69G>T
|
|
|
NM_001128225.2:c.1072G>T
|
NP_001121697.1:p.Ala358Ser
|
|
|
NM_152264.4:c.1051G>T
|
NP_689477.2:p.Ala351Ser
|
|
|
XM_006718381.2:c.1096G>T
|
XP_006718444.1:p.Ala366Ser
|
|
|
XM_006718383.2:c.988G>T
|
XP_006718446.1:p.Ala330Ser
|
|
|
XM_006718384.2:c.*69G>T
|
XP_006718447.1:n.*69G>T
|
|
|
XM_006718385.2:c.*69G>T
|
XP_006718448.1:n.*69G>T
|
|
|
XM_011520466.1:c.1117G>T
|
XP_011518768.1:p.Ala373Ser
|
|
|
XM_011520467.1:c.1072G>T
|
XP_011518769.1:p.Ala358Ser
|
|
|
XM_011520468.1:c.1072G>T
|
XP_011518770.1:p.Ala358Ser
|
|
|
XM_011520469.1:c.1009G>T
|
XP_011518771.1:p.Ala337Ser
|
|
|
XM_011520470.1:c.964G>T
|
XP_011518772.1:p.Ala322Ser
|
|
|
XR_242832.1:n.1457G>T
|
|
|
|
XR_428862.2:n.1132G>T
|
|
|
|
XR_428863.2:n.1128G>T
|
|
|
|
XR_930928.1:n.1153G>T
|
|
|
|
NM_001330245.1:c.*69G>T
|
NP_001317174.1:n.*69G>T
|
|
|
NR_134854.1:n.1313G>T
|
|
|
|
XM_006718381.3:c.1096G>T
|
XP_006718444.1:p.Ala366Ser
|
|
|
XM_006718383.3:c.988G>T
|
XP_006718446.1:p.Ala330Ser
|
|
|
XM_011520468.3:c.1072G>T
|
XP_011518770.1:p.Ala358Ser
|
|
|
XM_011520470.2:c.964G>T
|
XP_011518772.1:p.Ala322Ser
|
|
|
XM_017018540.2:c.1051G>T
|
XP_016874029.1:p.Ala351Ser
|
|
|
XM_017018541.2:c.943G>T
|
XP_016874030.1:p.Ala315Ser
|
|
|
XM_024448762.1:c.1201G>T
|
XP_024304530.1:p.Ala401Ser
|
|
|
XR_001748027.1:n.1272G>T
|
|
|
|
XR_001748028.1:n.1254G>T
|
|
|
|
XR_428862.3:n.1132G>T
|
|
|
|
XR_428863.3:n.1128G>T
|
|
|
|
XR_930928.2:n.1153G>T
|
|
|
|
NM_001128225.3:c.1072G>T
MANE Select
|
NP_001121697.2:p.Ala358Ser
|
|
|
NM_001330245.2:c.*69G>T
|
NP_001317174.2:n.*69G>T
|
|
|
NM_152264.5:c.1051G>T
|
NP_689477.3:p.Ala351Ser
|
|
