ENST00000355808.10:c.764T>C
|
ENSP00000348062.6:p.Phe255Ser
|
|
ENST00000379805.4:c.*435T>C
|
ENSP00000369133.3:n.*435T>C
|
|
ENST00000417819.6:c.827T>C
|
ENSP00000404616.2:p.Phe276Ser
|
|
ENST00000423505.6:c.857T>C
|
ENSP00000406473.2:p.Phe286Ser
|
|
ENST00000481733.2:n.538T>C
|
|
|
ENST00000696704.1:c.*75T>C
|
ENSP00000512823.1:n.*75T>C
|
|
ENST00000696705.1:c.*198T>C
|
ENSP00000512824.1:n.*198T>C
|
|
ENST00000422285.7:c.743T>C
MANE Select
|
ENSP00000394382.2:p.Phe248Ser
|
|
ENST00000379806.9:c.857T>C
|
ENSP00000369134.5:p.Phe286Ser
|
|
ENST00000422285.6:c.743T>C
|
ENSP00000394382.2:p.Phe248Ser
|
|
ENST00000481733.1:n.171T>C
|
|
|
ENST00000540249.5:c.650T>C
|
ENSP00000440761.1:p.Phe217Ser
|
|
ENST00000545074.5:c.764T>C
|
ENSP00000438550.1:p.Phe255Ser
|
|
NM_000284.3:c.743T>C
|
NP_000275.1:p.Phe248Ser
|
|
NM_001173454.1:c.857T>C
|
NP_001166925.1:p.Phe286Ser
|
|
NM_001173455.1:c.764T>C
|
NP_001166926.1:p.Phe255Ser
|
|
NM_001173456.1:c.650T>C
|
NP_001166927.1:p.Phe217Ser
|
|
XM_011545531.1:c.878T>C
|
XP_011543833.1:p.Phe293Ser
|
|
XM_011545532.1:c.785T>C
|
XP_011543834.1:p.Phe262Ser
|
|
XM_017029574.2:c.764T>C
|
XP_016885063.1:p.Phe255Ser
|
|
NM_000284.4:c.743T>C
MANE Select
|
NP_000275.1:p.Phe248Ser
|
|
NM_001173454.2:c.857T>C
|
NP_001166925.1:p.Phe286Ser
|
|
NM_001173455.2:c.764T>C
|
NP_001166926.1:p.Phe255Ser
|
|
NM_001173456.2:c.650T>C
|
NP_001166927.1:p.Phe217Ser
|
|