ENST00000394817.7:c.299G>C
MANE Select
|
ENSP00000378294.2:p.Arg100Thr
|
|
ENST00000265195.9:c.299G>C
|
ENSP00000265195.5:p.Arg100Thr
|
|
ENST00000394817.6:c.299G>C
|
ENSP00000378294.2:p.Arg100Thr
|
|
ENST00000503732.1:n.126G>C
|
|
|
ENST00000505830.5:c.329G>C
|
ENSP00000426460.1:p.Arg110Thr
|
|
ENST00000507002.5:c.329G>C
|
ENSP00000421890.1:p.Arg110Thr
|
|
ENST00000508639.5:c.299G>C
|
ENSP00000427371.1:p.Arg100Thr
|
|
ENST00000509534.5:c.320G>C
|
ENSP00000426858.1:p.Arg107Thr
|
|
ENST00000513453.5:c.299G>C
|
ENSP00000424014.1:p.Arg100Thr
|
|
NM_001037633.1:c.299G>C
|
NP_001032722.1:p.Arg100Thr
|
|
NM_022464.4:c.299G>C
|
NP_071909.1:p.Arg100Thr
|
|
XM_011543570.1:c.329G>C
|
XP_011541872.1:p.Arg110Thr
|
|
XM_011543570.2:c.329G>C
|
XP_011541872.1:p.Arg110Thr
|
|
XM_024446164.1:c.299G>C
|
XP_024301932.1:p.Arg100Thr
|
|
NM_022464.5:c.299G>C
MANE Select
|
NP_071909.1:p.Arg100Thr
|
|
NM_001037633.2:c.299G>C
|
NP_001032722.1:p.Arg100Thr
|
|