|
ENST00000371418.9:c.673+126A=
MANE Select
|
ENSP00000360472.4:n.673+126A=
|
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ENST00000485458.3:n.4649+126A=
|
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ENST00000635953.1:c.673+126A=
|
ENSP00000490058.1:n.673+126A=
|
|
|
ENST00000636155.1:c.673+126A=
|
ENSP00000490355.1:n.673+126A=
|
|
|
ENST00000636232.1:c.*459+126A=
|
ENSP00000490325.1:n.*459+126A=
|
|
|
ENST00000636754.1:c.*515+126A=
|
ENSP00000489781.1:n.*515+126A=
|
|
|
ENST00000636946.1:c.*842+126A=
|
ENSP00000490654.1:n.*842+126A=
|
|
|
ENST00000637037.1:c.*263+126A=
|
ENSP00000490860.1:n.*263+126A=
|
|
|
ENST00000637347.1:n.534+126A=
|
|
|
|
ENST00000637611.1:c.*229+126A=
|
ENSP00000489682.1:n.*229+126A=
|
|
|
ENST00000637689.1:c.-699+126A=
|
ENSP00000490496.1:n.-699+126A=
|
|
|
ENST00000637925.1:c.*268+126A=
|
ENSP00000489763.1:n.*268+126A=
|
|
|
ENST00000638049.1:c.*431+126A=
|
ENSP00000490597.1:n.*431+126A=
|
|
|
ENST00000676175.1:n.2412+126A=
|
|
|
|
ENST00000371413.4:c.673+126A=
|
ENSP00000360467.3:n.673+126A=
|
|
|
ENST00000371418.8:c.673+126A=
|
ENSP00000360472.4:n.673+126A=
|
|
|
ENST00000626307.1:n.4588+126A=
|
|
|
|
ENST00000626946.1:n.196A=
|
|
|
|
ENST00000627420.2:c.*382+126A=
|
ENSP00000487116.1:n.*382+126A=
|
|
|
ENST00000629035.2:c.601+126A=
|
ENSP00000486908.1:n.601+126A=
|
|
|
ENST00000630047.2:c.529+126A=
|
ENSP00000485917.1:n.529+126A=
|
|
|
ENST00000630412.1:n.461+126A=
|
|
|
|
ENST00000630487.2:c.*463+126A=
|
ENSP00000486859.1:n.*463+126A=
|
|
|
NM_001308275.1:c.673+126A=
|
NP_001295204.1:n.673+126A=
|
|
|
NM_001308276.1:c.529+126A=
|
NP_001295205.1:n.529+126A=
|
|
|
NM_005097.2:c.673+126A=
|
NP_005088.1:n.673+126A=
|
|
|
NM_005097.3:c.673+126A=
|
NP_005088.1:n.673+126A=
|
|
|
NR_131777.1:n.937+126A=
|
|
|
|
XM_017016911.2:c.673+126A=
|
XP_016872400.1:n.673+126A=
|
|
|
XM_017016912.2:c.529+126A=
|
XP_016872401.1:n.529+126A=
|
|
|
NM_005097.4:c.673+126A=
MANE Select
|
NP_005088.1:n.673+126A=
|
|
|
NM_001308275.2:c.673+126A=
|
NP_001295204.1:n.673+126A=
|
|
|
NM_001308276.2:c.529+126A=
|
NP_001295205.1:n.529+126A=
|
|
|
NR_131777.2:n.810+126A=
|
|
|
