ENST00000375262.4:c.783G>C
|
ENSP00000364411.2:p.Ter261Tyr
|
|
ENST00000375263.8:c.933G>C
MANE Select
|
ENSP00000364412.3:p.Ter311Tyr
|
|
ENST00000463517.2:n.2475G>C
|
|
|
ENST00000464104.6:n.1871G>C
|
|
|
ENST00000467499.6:c.*632G>C
|
ENSP00000498077.1:n.*632G>C
|
|
ENST00000494814.6:n.483G>C
|
|
|
ENST00000643789.1:c.3225G>C
|
|
|
ENST00000375262.3:c.783G>C
|
ENSP00000364411.2:p.Ter261Tyr
|
|
ENST00000375263.7:c.933G>C
|
ENSP00000364412.3:p.Ter311Tyr
|
|
ENST00000464104.5:n.786G>C
|
|
|
ENST00000467499.5:n.193G>C
|
|
|
ENST00000494814.5:n.492G>C
|
|
|
NM_000197.1:c.933G>C
|
NP_000188.1:p.Ter311Tyr
|
|
XM_005251970.3:c.573G>C
|
XP_005252027.1:p.Ter191Tyr
|
|
XM_011518618.1:c.933G>C
|
XP_011516920.1:p.Ter311Tyr
|
|
XM_011518619.1:c.933G>C
|
XP_011516921.1:p.Ter311Tyr
|
|
XM_011518620.1:c.825G>C
|
XP_011516922.1:p.Ter275Tyr
|
|
NM_000197.2:c.933G>C
MANE Select
|
NP_000188.1:p.Ter311Tyr
|
|
XM_011518618.2:c.933G>C
|
XP_011516920.1:p.Ter311Tyr
|
|
XM_011518619.2:c.933G>C
|
XP_011516921.1:p.Ter311Tyr
|
|
XM_017014671.1:c.933G>C
|
XP_016870160.1:p.Ter311Tyr
|
|
XM_017014672.1:c.933G>C
|
XP_016870161.1:p.Ter311Tyr
|
|
XM_017014673.2:c.897G>C
|
XP_016870162.1:p.Ter299Tyr
|
|
XM_017014674.1:c.825G>C
|
XP_016870163.1:p.Ter275Tyr
|
|
XM_017014675.1:c.771G>C
|
XP_016870164.1:p.Ter257Tyr
|
|
XM_017014677.1:c.573G>C
|
XP_016870166.1:p.Ter191Tyr
|
|
XM_024447529.1:c.771G>C
|
XP_024303297.1:p.Ter257Tyr
|
|
XR_002956778.1:n.3405G>C
|
|
|