ENST00000592092.2:n.520G>A
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|
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ENST00000673918.2:c.6148G>A
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ENSP00000501283.1:p.Ala2050Thr
|
|
ENST00000674114.2:c.3755G>A
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ENSP00000501039.2:n.3755G>A
|
|
ENST00000684977.1:c.1432G>A
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ENSP00000509384.1:p.Ala478Thr
|
|
ENST00000689544.1:n.1367G>A
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|
|
ENST00000691421.1:c.1435G>A
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ENSP00000508674.1:p.Ala479Thr
|
|
ENST00000691855.1:c.5756G>A
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|
|
ENST00000692961.1:c.6214G>A
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ENSP00000509289.1:p.Ala2072Thr
|
|
ENST00000693677.1:c.704+434G>A
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ENSP00000509779.1:n.704+434G>A
|
|
ENST00000420124.4:c.6214G>A
MANE Select
|
ENSP00000398837.2:p.Ala2072Thr
|
|
ENST00000673918.1:c.6148G>A
|
ENSP00000501283.1:p.Ala2050Thr
|
|
ENST00000674114.1:c.3536G>A
|
|
|
ENST00000420124.2:c.6214G>A
|
ENSP00000398837.1:p.Ala2072Thr
|
|
NM_014727.2:c.6214G>A
|
NP_055542.1:p.Ala2072Thr
|
|
XM_011527561.1:c.6148G>A
|
XP_011525863.1:p.Ala2050Thr
|
|
XM_011527562.1:c.6214G>A
|
XP_011525864.1:p.Ala2072Thr
|
|
XM_011527563.1:c.5938G>A
|
XP_011525865.1:p.Ala1980Thr
|
|
XM_011527561.2:c.5650G>A
|
XP_011525863.2:p.Ala1884Thr
|
|
XM_011527562.2:c.6214G>A
|
XP_011525864.1:p.Ala2072Thr
|
|
XM_017027544.1:c.6214G>A
|
XP_016883033.1:p.Ala2072Thr
|
|
XM_017027545.1:c.5650G>A
|
XP_016883034.1:p.Ala1884Thr
|
|
XM_017027546.1:c.3178G>A
|
XP_016883035.1:p.Ala1060Thr
|
|
NM_014727.3:c.6214G>A
MANE Select
|
NP_055542.1:p.Ala2072Thr
|
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