ENST00000692585.1:c.1116A>C
|
ENSP00000509200.1:p.Ter372Cys
|
|
ENST00000294309.8:c.2259A>C
MANE Select
|
ENSP00000294309.3:p.Ter753Cys
|
|
ENST00000635811.1:c.*454A>C
|
ENSP00000490341.1:n.*454A>C
|
|
ENST00000637084.1:c.1116A>C
|
ENSP00000490615.1:p.Ter372Cys
|
|
ENST00000637342.1:c.2003+2023A>C
|
ENSP00000490171.1:n.2003+2023A>C
|
|
ENST00000637504.1:c.*33+2667A>C
|
ENSP00000489759.1:n.*33+2667A>C
|
|
ENST00000294309.7:c.2259A>C
|
ENSP00000294309.3:p.Ter753Cys
|
|
ENST00000442692.2:n.1725A>C
|
|
|
ENST00000542467.1:c.1713A>C
|
ENSP00000445551.1:p.Ter571Cys
|
|
NM_139075.3:c.2259A>C
|
NP_620714.2:p.Ter753Cys
|
|
XM_005273824.2:c.2256A>C
|
XP_005273881.1:p.Ter752Cys
|
|
XM_005273826.2:c.2004A>C
|
XP_005273883.1:p.Ter668Cys
|
|
XM_005273830.2:c.1566A>C
|
XP_005273887.1:p.Ter522Cys
|
|
XM_005273831.2:c.1566A>C
|
XP_005273888.1:p.Ter522Cys
|
|
XM_005273832.2:c.1536A>C
|
XP_005273889.1:p.Ter512Cys
|
|
XM_006718453.2:c.1639+6454A>C
|
XP_006718516.1:n.1639+6454A>C
|
|
XM_006718454.2:c.1689+6454A>C
|
XP_006718517.1:n.1689+6454A>C
|
|
XM_011544802.1:c.2019A>C
|
XP_011543104.1:p.Ter673Cys
|
|
XM_011544807.1:c.1563A>C
|
XP_011543109.1:p.Ter521Cys
|
|
XM_011544808.1:c.1428A>C
|
XP_011543110.1:p.Ter476Cys
|
|
XM_005273824.4:c.2256A>C
|
XP_005273881.1:p.Ter752Cys
|
|
XM_005273826.4:c.2004A>C
|
XP_005273883.1:p.Ter668Cys
|
|
XM_005273830.4:c.1566A>C
|
XP_005273887.1:p.Ter522Cys
|
|
XM_005273831.4:c.1566A>C
|
XP_005273888.1:p.Ter522Cys
|
|
XM_005273832.4:c.1536A>C
|
XP_005273889.1:p.Ter512Cys
|
|
XM_011544802.3:c.2019A>C
|
XP_011543104.1:p.Ter673Cys
|
|
XM_011544807.3:c.1563A>C
|
XP_011543109.1:p.Ter521Cys
|
|
XM_011544808.3:c.1428A>C
|
XP_011543110.1:p.Ter476Cys
|
|
XM_017017328.2:c.2040A>C
|
XP_016872817.1:p.Ter680Cys
|
|
XM_017017329.2:c.2037A>C
|
XP_016872818.1:p.Ter679Cys
|
|
XM_017017330.2:c.1536A>C
|
XP_016872819.1:p.Ter512Cys
|
|
XM_017017331.2:c.1536A>C
|
XP_016872820.1:p.Ter512Cys
|
|
XM_017017332.2:c.1350A>C
|
XP_016872821.1:p.Ter450Cys
|
|
XM_017017333.2:c.1317A>C
|
XP_016872822.1:p.Ter439Cys
|
|
XM_017017334.2:c.1317A>C
|
XP_016872823.1:p.Ter439Cys
|
|
XM_017017335.2:c.1317A>C
|
XP_016872824.1:p.Ter439Cys
|
|
XM_017017336.2:c.1209A>C
|
XP_016872825.1:p.Ter403Cys
|
|
XM_024448392.1:c.2049A>C
|
XP_024304160.1:p.Ter683Cys
|
|
XM_024448393.1:c.1536A>C
|
XP_024304161.1:p.Ter512Cys
|
|
XR_001747789.2:n.2191A>C
|
|
|
XR_247191.3:n.2313A>C
|
|
|
NM_139075.4:c.2259A>C
MANE Select
|
NP_620714.2:p.Ter753Cys
|
|