ENST00000375262.4:c.728G>T
|
ENSP00000364411.2:p.Arg243Met
|
|
ENST00000375263.8:c.878G>T
MANE Select
|
ENSP00000364412.3:p.Arg293Met
|
|
ENST00000463517.2:n.2420G>T
|
|
|
ENST00000464104.6:n.1816G>T
|
|
|
ENST00000467499.6:c.*577G>T
|
ENSP00000498077.1:n.*577G>T
|
|
ENST00000494814.6:n.428G>T
|
|
|
ENST00000643789.1:c.3170G>T
|
|
|
ENST00000648146.1:c.1016G>T
|
ENSP00000497238.1:n.1016G>T
|
|
ENST00000648332.1:c.555G>T
|
ENSP00000497562.1:n.555G>T
|
|
ENST00000650005.1:c.807G>T
|
ENSP00000498121.1:n.807G>T
|
|
ENST00000375262.3:c.728G>T
|
ENSP00000364411.2:p.Arg243Met
|
|
ENST00000375263.7:c.878G>T
|
ENSP00000364412.3:p.Arg293Met
|
|
ENST00000464104.5:n.731G>T
|
|
|
ENST00000467499.5:n.138G>T
|
|
|
ENST00000494814.5:n.437G>T
|
|
|
NM_000197.1:c.878G>T
|
NP_000188.1:p.Arg293Met
|
|
XM_005251970.3:c.518G>T
|
XP_005252027.1:p.Arg173Met
|
|
XM_011518618.1:c.878G>T
|
XP_011516920.1:p.Arg293Met
|
|
XM_011518619.1:c.878G>T
|
XP_011516921.1:p.Arg293Met
|
|
XM_011518620.1:c.770G>T
|
XP_011516922.1:p.Arg257Met
|
|
NM_000197.2:c.878G>T
MANE Select
|
NP_000188.1:p.Arg293Met
|
|
XM_011518618.2:c.878G>T
|
XP_011516920.1:p.Arg293Met
|
|
XM_011518619.2:c.878G>T
|
XP_011516921.1:p.Arg293Met
|
|
XM_017014671.1:c.878G>T
|
XP_016870160.1:p.Arg293Met
|
|
XM_017014672.1:c.878G>T
|
XP_016870161.1:p.Arg293Met
|
|
XM_017014673.2:c.842G>T
|
XP_016870162.1:p.Arg281Met
|
|
XM_017014674.1:c.770G>T
|
XP_016870163.1:p.Arg257Met
|
|
XM_017014675.1:c.716G>T
|
XP_016870164.1:p.Arg239Met
|
|
XM_017014677.1:c.518G>T
|
XP_016870166.1:p.Arg173Met
|
|
XM_024447529.1:c.716G>T
|
XP_024303297.1:p.Arg239Met
|
|
XR_002956778.1:n.3350G>T
|
|
|