ENST00000674709.1:c.*2814T>C
|
ENSP00000502092.1:n.*2814T>C
|
|
ENST00000674736.1:c.*2643T>C
|
ENSP00000501873.1:n.*2643T>C
|
|
ENST00000675039.1:c.3287T>C
|
ENSP00000501574.1:p.Met1096Thr
|
|
ENST00000675850.1:c.3287T>C
MANE Select
|
ENSP00000502357.1:p.Met1096Thr
|
|
ENST00000675961.1:c.3287T>C
|
ENSP00000501808.1:p.Met1096Thr
|
|
ENST00000676139.1:c.*2620T>C
|
ENSP00000502496.1:n.*2620T>C
|
|
ENST00000284476.7:c.3287T>C
|
ENSP00000284476.6:p.Met1096Thr
|
|
NM_032890.3:c.3287T>C
|
NP_116279.2:p.Met1096Thr
|
|
XM_005273335.1:c.3287T>C
|
XP_005273392.1:p.Met1096Thr
|
|
XM_006711592.1:c.3287T>C
|
XP_006711655.1:p.Met1096Thr
|
|
XM_006711594.2:c.2705T>C
|
XP_006711657.1:p.Met902Thr
|
|
XM_011510072.1:c.3287T>C
|
XP_011508374.1:p.Met1096Thr
|
|
XM_011510073.1:c.3287T>C
|
XP_011508375.1:p.Met1096Thr
|
|
XM_011510074.1:c.3287T>C
|
XP_011508376.1:p.Met1096Thr
|
|
XM_011510075.1:c.3287T>C
|
XP_011508377.1:p.Met1096Thr
|
|
XM_011510076.1:c.3287T>C
|
XP_011508378.1:p.Met1096Thr
|
|
XM_011510077.1:c.3287T>C
|
XP_011508379.1:p.Met1096Thr
|
|
XM_011510078.1:c.2705T>C
|
XP_011508380.1:p.Met902Thr
|
|
NM_001350630.1:c.2558T>C
|
NP_001337559.1:p.Met853Thr
|
|
NM_032890.4:c.3287T>C
|
NP_116279.2:p.Met1096Thr
|
|
XM_005273335.2:c.3287T>C
|
XP_005273392.1:p.Met1096Thr
|
|
XM_006711592.2:c.3287T>C
|
XP_006711655.1:p.Met1096Thr
|
|
XM_006711594.3:c.2705T>C
|
XP_006711657.1:p.Met902Thr
|
|
XM_011510072.2:c.3287T>C
|
XP_011508374.1:p.Met1096Thr
|
|
XM_011510073.2:c.3287T>C
|
XP_011508375.1:p.Met1096Thr
|
|
XM_011510074.2:c.3287T>C
|
XP_011508376.1:p.Met1096Thr
|
|
XM_011510075.2:c.3287T>C
|
XP_011508377.1:p.Met1096Thr
|
|
XM_011510077.2:c.3287T>C
|
XP_011508379.1:p.Met1096Thr
|
|
XM_017002611.1:c.3287T>C
|
XP_016858100.1:p.Met1096Thr
|
|
XM_017002612.1:c.2705T>C
|
XP_016858101.1:p.Met902Thr
|
|
NM_001350630.2:c.2558T>C
|
NP_001337559.1:p.Met853Thr
|
|
NM_001369594.1:c.3287T>C
|
NP_001356523.1:p.Met1096Thr
|
|
NM_001377228.1:c.3287T>C
|
NP_001364157.1:p.Met1096Thr
|
|
NM_001377229.1:c.3287T>C
MANE Select
|
NP_001364158.1:p.Met1096Thr
|
|
NM_032890.5:c.3287T>C
|
NP_116279.2:p.Met1096Thr
|
|