|
ENST00000371418.9:c.679G>T
MANE Select
|
ENSP00000360472.4:p.Ala227Ser
|
|
|
ENST00000485458.3:n.4655G>T
|
|
|
|
ENST00000635953.1:c.679G>T
|
ENSP00000490058.1:p.Ala227Ser
|
|
|
ENST00000636155.1:c.679G>T
|
ENSP00000490355.1:p.Ala227Ser
|
|
|
ENST00000636232.1:c.*465G>T
|
ENSP00000490325.1:n.*465G>T
|
|
|
ENST00000636754.1:c.*521G>T
|
ENSP00000489781.1:n.*521G>T
|
|
|
ENST00000636946.1:c.*848G>T
|
ENSP00000490654.1:n.*848G>T
|
|
|
ENST00000637037.1:c.*269G>T
|
ENSP00000490860.1:n.*269G>T
|
|
|
ENST00000637347.1:n.540G>T
|
|
|
|
ENST00000637611.1:c.*235G>T
|
ENSP00000489682.1:n.*235G>T
|
|
|
ENST00000637689.1:c.-693G>T
|
ENSP00000490496.1:n.-693G>T
|
|
|
ENST00000637925.1:c.*274G>T
|
ENSP00000489763.1:n.*274G>T
|
|
|
ENST00000638049.1:c.*437G>T
|
ENSP00000490597.1:n.*437G>T
|
|
|
ENST00000676175.1:n.2418G>T
|
|
|
|
ENST00000371413.4:c.679G>T
|
ENSP00000360467.3:p.Ala227Ser
|
|
|
ENST00000371418.8:c.679G>T
|
ENSP00000360472.4:p.Ala227Ser
|
|
|
ENST00000626307.1:n.4594G>T
|
|
|
|
ENST00000626946.1:n.349G>T
|
|
|
|
ENST00000627420.2:c.*388G>T
|
ENSP00000487116.1:n.*388G>T
|
|
|
ENST00000629035.2:c.607G>T
|
ENSP00000486908.1:p.Ala203Ser
|
|
|
ENST00000630047.2:c.535G>T
|
ENSP00000485917.1:p.Ala179Ser
|
|
|
ENST00000630412.1:n.467G>T
|
|
|
|
ENST00000630487.2:c.*469G>T
|
ENSP00000486859.1:n.*469G>T
|
|
|
NM_001308275.1:c.679G>T
|
NP_001295204.1:p.Ala227Ser
|
|
|
NM_001308276.1:c.535G>T
|
NP_001295205.1:p.Ala179Ser
|
|
|
NM_005097.2:c.679G>T
|
NP_005088.1:p.Ala227Ser
|
|
|
NM_005097.3:c.679G>T
|
NP_005088.1:p.Ala227Ser
|
|
|
NR_131777.1:n.943G>T
|
|
|
|
XM_017016911.2:c.679G>T
|
XP_016872400.1:p.Ala227Ser
|
|
|
XM_017016912.2:c.535G>T
|
XP_016872401.1:p.Ala179Ser
|
|
|
NM_005097.4:c.679G>T
MANE Select
|
NP_005088.1:p.Ala227Ser
|
|
|
NM_001308275.2:c.679G>T
|
NP_001295204.1:p.Ala227Ser
|
|
|
NM_001308276.2:c.535G>T
|
NP_001295205.1:p.Ala179Ser
|
|
|
NR_131777.2:n.816G>T
|
|
|
