ENST00000247933.9:c.803G>C
|
ENSP00000247933.4:p.Ser268Thr
|
|
ENST00000514224.2:c.803G>C
MANE Select
|
ENSP00000425081.2:p.Ser268Thr
|
|
ENST00000652070.1:n.859G>C
|
|
|
ENST00000247933.8:c.803G>C
|
ENSP00000247933.4:p.Ser268Thr
|
|
ENST00000502910.5:c.662G>C
|
ENSP00000422952.1:p.Ser221Thr
|
|
ENST00000514192.5:c.620G>C
|
ENSP00000423685.1:p.Ser207Thr
|
|
ENST00000514224.1:c.407G>C
|
ENSP00000425081.1:p.Ser136Thr
|
|
ENST00000514698.5:n.803G>C
|
|
|
NM_000203.4:c.803G>C
|
NP_000194.2:p.Ser268Thr
|
|
NR_110313.1:n.891G>C
|
|
|
XM_006713882.2:c.407G>C
|
XP_006713945.1:p.Ser136Thr
|
|
XM_011513459.1:c.762G>C
|
XP_011511761.1:p.Gln254His
|
|
XM_011513460.1:c.662G>C
|
XP_011511762.1:p.Ser221Thr
|
|
XM_011513461.1:c.596G>C
|
XP_011511763.1:p.Ser199Thr
|
|
XM_011513462.1:c.515G>C
|
XP_011511764.1:p.Ser172Thr
|
|
XM_011513463.1:c.515G>C
|
XP_011511765.1:p.Ser172Thr
|
|
XR_924947.1:n.872G>C
|
|
|
NM_000203.5:c.803G>C
MANE Select
|
NP_000194.2:p.Ser268Thr
|
|
NM_001363576.1:c.407G>C
|
NP_001350505.1:p.Ser136Thr
|
|
XM_011513461.2:c.596G>C
|
XP_011511763.1:p.Ser199Thr
|
|
XM_017008163.1:c.-158G>C
|
XP_016863652.1:n.-158G>C
|
|