ENST00000375262.4:c.751G>A
|
ENSP00000364411.2:p.Ala251Thr
|
|
ENST00000375263.8:c.901G>A
MANE Select
|
ENSP00000364412.3:p.Ala301Thr
|
|
ENST00000463517.2:n.2443G>A
|
|
|
ENST00000464104.6:n.1839G>A
|
|
|
ENST00000467499.6:c.*600G>A
|
ENSP00000498077.1:n.*600G>A
|
|
ENST00000494814.6:n.451G>A
|
|
|
ENST00000643789.1:c.3193G>A
|
|
|
ENST00000648146.1:c.1039G>A
|
ENSP00000497238.1:n.1039G>A
|
|
ENST00000648332.1:c.578G>A
|
ENSP00000497562.1:n.578G>A
|
|
ENST00000650005.1:c.830G>A
|
ENSP00000498121.1:n.830G>A
|
|
ENST00000375262.3:c.751G>A
|
ENSP00000364411.2:p.Ala251Thr
|
|
ENST00000375263.7:c.901G>A
|
ENSP00000364412.3:p.Ala301Thr
|
|
ENST00000464104.5:n.754G>A
|
|
|
ENST00000467499.5:n.161G>A
|
|
|
ENST00000494814.5:n.460G>A
|
|
|
NM_000197.1:c.901G>A
|
NP_000188.1:p.Ala301Thr
|
|
XM_005251970.3:c.541G>A
|
XP_005252027.1:p.Ala181Thr
|
|
XM_011518618.1:c.901G>A
|
XP_011516920.1:p.Ala301Thr
|
|
XM_011518619.1:c.901G>A
|
XP_011516921.1:p.Ala301Thr
|
|
XM_011518620.1:c.793G>A
|
XP_011516922.1:p.Ala265Thr
|
|
NM_000197.2:c.901G>A
MANE Select
|
NP_000188.1:p.Ala301Thr
|
|
XM_011518618.2:c.901G>A
|
XP_011516920.1:p.Ala301Thr
|
|
XM_011518619.2:c.901G>A
|
XP_011516921.1:p.Ala301Thr
|
|
XM_017014671.1:c.901G>A
|
XP_016870160.1:p.Ala301Thr
|
|
XM_017014672.1:c.901G>A
|
XP_016870161.1:p.Ala301Thr
|
|
XM_017014673.2:c.865G>A
|
XP_016870162.1:p.Ala289Thr
|
|
XM_017014674.1:c.793G>A
|
XP_016870163.1:p.Ala265Thr
|
|
XM_017014675.1:c.739G>A
|
XP_016870164.1:p.Ala247Thr
|
|
XM_017014677.1:c.541G>A
|
XP_016870166.1:p.Ala181Thr
|
|
XM_024447529.1:c.739G>A
|
XP_024303297.1:p.Ala247Thr
|
|
XR_002956778.1:n.3373G>A
|
|
|