ENST00000330684.4:c.929T>C
MANE Select
|
ENSP00000332549.3:p.Phe310Ser
|
|
ENST00000535259.6:c.458T>C
|
ENSP00000441572.3:p.Phe153Ser
|
|
ENST00000636273.2:n.522T>C
|
|
|
ENST00000637393.1:c.521T>C
|
ENSP00000490232.1:p.Phe174Ser
|
|
ENST00000674742.1:c.458T>C
|
ENSP00000502200.1:p.Phe153Ser
|
|
ENST00000675189.1:n.1413T>C
|
|
|
ENST00000675398.1:c.929T>C
|
ENSP00000502752.1:p.Phe310Ser
|
|
ENST00000330684.3:c.929T>C
|
ENSP00000332549.3:p.Phe310Ser
|
|
ENST00000396573.6:c.929T>C
|
ENSP00000379818.2:p.Phe310Ser
|
|
ENST00000396575.6:c.518T>C
|
ENSP00000379820.3:p.Phe173Ser
|
|
ENST00000461292.3:n.568T>C
|
|
|
ENST00000535259.5:c.518T>C
|
ENSP00000441572.2:p.Phe173Ser
|
|
ENST00000562109.5:c.929T>C
|
ENSP00000454998.1:p.Phe310Ser
|
|
ENST00000566683.1:n.241-46937T>C
|
|
|
ENST00000568247.3:n.821T>C
|
|
|
NM_000833.4:c.929T>C
|
NP_000824.1:p.Phe310Ser
|
|
NM_001134407.2:c.929T>C
|
NP_001127879.1:p.Phe310Ser
|
|
NM_001134408.2:c.929T>C
|
NP_001127880.1:p.Phe310Ser
|
|
XM_011522456.1:c.770T>C
|
XP_011520758.1:p.Phe257Ser
|
|
XM_011522457.1:c.671T>C
|
XP_011520759.1:p.Phe224Ser
|
|
XM_011522458.1:c.458T>C
|
XP_011520760.1:p.Phe153Ser
|
|
XM_011522459.1:c.458T>C
|
XP_011520761.1:p.Phe153Ser
|
|
XM_011522460.1:c.458T>C
|
XP_011520762.1:p.Phe153Ser
|
|
XM_011522461.1:c.929T>C
|
XP_011520763.1:p.Phe310Ser
|
|
XM_011522458.3:c.458T>C
|
XP_011520760.1:p.Phe153Ser
|
|
XM_011522461.3:c.929T>C
|
XP_011520763.1:p.Phe310Ser
|
|
XM_017023172.1:c.1085T>C
|
XP_016878661.1:p.Phe362Ser
|
|
XM_017023173.1:c.1085T>C
|
XP_016878662.1:p.Phe362Ser
|
|
NM_001134407.3:c.929T>C
MANE Select
|
NP_001127879.1:p.Phe310Ser
|
|
NM_000833.5:c.929T>C
|
NP_000824.1:p.Phe310Ser
|
|