ENST00000375262.4:c.619G>T
|
ENSP00000364411.2:p.Ala207Ser
|
|
ENST00000375263.8:c.619G>T
MANE Select
|
ENSP00000364412.3:p.Ala207Ser
|
|
ENST00000463517.2:n.2161G>T
|
|
|
ENST00000464104.6:n.1557G>T
|
|
|
ENST00000467499.6:c.*318G>T
|
ENSP00000498077.1:n.*318G>T
|
|
ENST00000494814.6:n.131G>T
|
|
|
ENST00000643789.1:c.2911G>T
|
|
|
ENST00000648146.1:c.619G>T
|
ENSP00000497238.1:p.Ala207Ser
|
|
ENST00000648332.1:c.296G>T
|
ENSP00000497562.1:p.Arg99Leu
|
|
ENST00000648799.1:c.511G>T
|
ENSP00000498039.1:p.Ala171Ser
|
|
ENST00000650005.1:c.548G>T
|
ENSP00000498121.1:p.Arg183Leu
|
|
ENST00000375262.3:c.619G>T
|
ENSP00000364411.2:p.Ala207Ser
|
|
ENST00000375263.7:c.619G>T
|
ENSP00000364412.3:p.Ala207Ser
|
|
ENST00000464104.5:n.472G>T
|
|
|
ENST00000494814.5:n.140G>T
|
|
|
NM_000197.1:c.619G>T
|
NP_000188.1:p.Ala207Ser
|
|
XM_005251970.3:c.259G>T
|
XP_005252027.1:p.Ala87Ser
|
|
XM_011518618.1:c.619G>T
|
XP_011516920.1:p.Ala207Ser
|
|
XM_011518619.1:c.619G>T
|
XP_011516921.1:p.Ala207Ser
|
|
XM_011518620.1:c.511G>T
|
XP_011516922.1:p.Ala171Ser
|
|
XM_011518621.1:c.619G>T
|
XP_011516923.1:p.Ala207Ser
|
|
NM_000197.2:c.619G>T
MANE Select
|
NP_000188.1:p.Ala207Ser
|
|
XM_011518618.2:c.619G>T
|
XP_011516920.1:p.Ala207Ser
|
|
XM_011518619.2:c.619G>T
|
XP_011516921.1:p.Ala207Ser
|
|
XM_017014671.1:c.619G>T
|
XP_016870160.1:p.Ala207Ser
|
|
XM_017014672.1:c.619G>T
|
XP_016870161.1:p.Ala207Ser
|
|
XM_017014673.2:c.583G>T
|
XP_016870162.1:p.Ala195Ser
|
|
XM_017014674.1:c.511G>T
|
XP_016870163.1:p.Ala171Ser
|
|
XM_017014675.1:c.457G>T
|
XP_016870164.1:p.Ala153Ser
|
|
XM_017014677.1:c.259G>T
|
XP_016870166.1:p.Ala87Ser
|
|
XM_024447529.1:c.457G>T
|
XP_024303297.1:p.Ala153Ser
|
|
XR_002956778.1:n.3053G>T
|
|
|