ENST00000692585.1:c.1048G>T
|
ENSP00000509200.1:p.Glu350Ter
|
|
ENST00000294309.8:c.2191G>T
MANE Select
|
ENSP00000294309.3:p.Glu731Ter
|
|
ENST00000635811.1:c.*386G>T
|
ENSP00000490341.1:n.*386G>T
|
|
ENST00000637084.1:c.1048G>T
|
ENSP00000490615.1:p.Glu350Ter
|
|
ENST00000637342.1:c.2003+1955G>T
|
ENSP00000490171.1:n.2003+1955G>T
|
|
ENST00000637504.1:c.*33+2599G>T
|
ENSP00000489759.1:n.*33+2599G>T
|
|
ENST00000294309.7:c.2191G>T
|
ENSP00000294309.3:p.Glu731Ter
|
|
ENST00000442692.2:n.1657G>T
|
|
|
ENST00000542467.1:c.1645G>T
|
ENSP00000445551.1:p.Glu549Ter
|
|
NM_139075.3:c.2191G>T
|
NP_620714.2:p.Glu731Ter
|
|
XM_005273824.2:c.2188G>T
|
XP_005273881.1:p.Glu730Ter
|
|
XM_005273826.2:c.1936G>T
|
XP_005273883.1:p.Glu646Ter
|
|
XM_005273830.2:c.1498G>T
|
XP_005273887.1:p.Glu500Ter
|
|
XM_005273831.2:c.1498G>T
|
XP_005273888.1:p.Glu500Ter
|
|
XM_005273832.2:c.1468G>T
|
XP_005273889.1:p.Glu490Ter
|
|
XM_006718453.2:c.1639+6386G>T
|
XP_006718516.1:n.1639+6386G>T
|
|
XM_006718454.2:c.1689+6386G>T
|
XP_006718517.1:n.1689+6386G>T
|
|
XM_011544802.1:c.1951G>T
|
XP_011543104.1:p.Glu651Ter
|
|
XM_011544807.1:c.1495G>T
|
XP_011543109.1:p.Glu499Ter
|
|
XM_011544808.1:c.1360G>T
|
XP_011543110.1:p.Glu454Ter
|
|
XR_247191.1:n.2242G>T
|
|
|
XM_005273824.4:c.2188G>T
|
XP_005273881.1:p.Glu730Ter
|
|
XM_005273826.4:c.1936G>T
|
XP_005273883.1:p.Glu646Ter
|
|
XM_005273830.4:c.1498G>T
|
XP_005273887.1:p.Glu500Ter
|
|
XM_005273831.4:c.1498G>T
|
XP_005273888.1:p.Glu500Ter
|
|
XM_005273832.4:c.1468G>T
|
XP_005273889.1:p.Glu490Ter
|
|
XM_011544802.3:c.1951G>T
|
XP_011543104.1:p.Glu651Ter
|
|
XM_011544807.3:c.1495G>T
|
XP_011543109.1:p.Glu499Ter
|
|
XM_011544808.3:c.1360G>T
|
XP_011543110.1:p.Glu454Ter
|
|
XM_017017328.2:c.1972G>T
|
XP_016872817.1:p.Glu658Ter
|
|
XM_017017329.2:c.1969G>T
|
XP_016872818.1:p.Glu657Ter
|
|
XM_017017330.2:c.1468G>T
|
XP_016872819.1:p.Glu490Ter
|
|
XM_017017331.2:c.1468G>T
|
XP_016872820.1:p.Glu490Ter
|
|
XM_017017332.2:c.1282G>T
|
XP_016872821.1:p.Glu428Ter
|
|
XM_017017333.2:c.1249G>T
|
XP_016872822.1:p.Glu417Ter
|
|
XM_017017334.2:c.1249G>T
|
XP_016872823.1:p.Glu417Ter
|
|
XM_017017335.2:c.1249G>T
|
XP_016872824.1:p.Glu417Ter
|
|
XM_017017336.2:c.1141G>T
|
XP_016872825.1:p.Glu381Ter
|
|
XM_024448392.1:c.1981G>T
|
XP_024304160.1:p.Glu661Ter
|
|
XM_024448393.1:c.1468G>T
|
XP_024304161.1:p.Glu490Ter
|
|
XR_001747789.2:n.2123G>T
|
|
|
XR_247191.3:n.2245G>T
|
|
|
NM_139075.4:c.2191G>T
MANE Select
|
NP_620714.2:p.Glu731Ter
|
|