ENST00000375262.4:c.729G>C
|
ENSP00000364411.2:p.Arg243Ser
|
|
ENST00000375263.8:c.879G>C
MANE Select
|
ENSP00000364412.3:p.Arg293Ser
|
|
ENST00000463517.2:n.2421G>C
|
|
|
ENST00000464104.6:n.1817G>C
|
|
|
ENST00000467499.6:c.*578G>C
|
ENSP00000498077.1:n.*578G>C
|
|
ENST00000494814.6:n.429G>C
|
|
|
ENST00000643789.1:c.3171G>C
|
|
|
ENST00000648146.1:c.1017G>C
|
ENSP00000497238.1:n.1017G>C
|
|
ENST00000648332.1:c.556G>C
|
ENSP00000497562.1:n.556G>C
|
|
ENST00000650005.1:c.808G>C
|
ENSP00000498121.1:n.808G>C
|
|
ENST00000375262.3:c.729G>C
|
ENSP00000364411.2:p.Arg243Ser
|
|
ENST00000375263.7:c.879G>C
|
ENSP00000364412.3:p.Arg293Ser
|
|
ENST00000464104.5:n.732G>C
|
|
|
ENST00000467499.5:n.139G>C
|
|
|
ENST00000494814.5:n.438G>C
|
|
|
NM_000197.1:c.879G>C
|
NP_000188.1:p.Arg293Ser
|
|
XM_005251970.3:c.519G>C
|
XP_005252027.1:p.Arg173Ser
|
|
XM_011518618.1:c.879G>C
|
XP_011516920.1:p.Arg293Ser
|
|
XM_011518619.1:c.879G>C
|
XP_011516921.1:p.Arg293Ser
|
|
XM_011518620.1:c.771G>C
|
XP_011516922.1:p.Arg257Ser
|
|
NM_000197.2:c.879G>C
MANE Select
|
NP_000188.1:p.Arg293Ser
|
|
XM_011518618.2:c.879G>C
|
XP_011516920.1:p.Arg293Ser
|
|
XM_011518619.2:c.879G>C
|
XP_011516921.1:p.Arg293Ser
|
|
XM_017014671.1:c.879G>C
|
XP_016870160.1:p.Arg293Ser
|
|
XM_017014672.1:c.879G>C
|
XP_016870161.1:p.Arg293Ser
|
|
XM_017014673.2:c.843G>C
|
XP_016870162.1:p.Arg281Ser
|
|
XM_017014674.1:c.771G>C
|
XP_016870163.1:p.Arg257Ser
|
|
XM_017014675.1:c.717G>C
|
XP_016870164.1:p.Arg239Ser
|
|
XM_017014677.1:c.519G>C
|
XP_016870166.1:p.Arg173Ser
|
|
XM_024447529.1:c.717G>C
|
XP_024303297.1:p.Arg239Ser
|
|
XR_002956778.1:n.3351G>C
|
|
|