ENST00000525346.6:c.1153G>A
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ENSP00000435707.3:p.Ala385Thr
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ENST00000526780.6:c.1153G>A
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ENSP00000435668.2:p.Ala385Thr
|
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ENST00000527316.6:c.979G>A
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ENSP00000435047.2:p.Ala327Thr
|
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ENST00000682708.1:c.1204G>A
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ENSP00000506866.1:p.Ala402Thr
|
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ENST00000683287.1:c.1189G>A
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ENSP00000507607.1:p.Ala397Thr
|
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ENST00000683714.1:c.1161G>A
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ENSP00000508207.1:p.Pro387=
|
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ENST00000684396.1:n.1193G>A
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|
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ENST00000685320.1:c.568G>A
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ENSP00000509319.1:p.Ala190Thr
|
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ENST00000690257.1:c.1057G>A
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ENSP00000510750.1:p.Ala353Thr
|
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ENST00000355527.8:c.1153G>A
MANE Select
|
ENSP00000347717.4:p.Ala385Thr
|
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ENST00000355527.7:c.1153G>A
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ENSP00000347717.3:p.Ala385Thr
|
|
ENST00000407721.6:c.1153G>A
|
ENSP00000384739.2:p.Ala385Thr
|
|
ENST00000525137.1:c.654G>A
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ENSP00000435956.1:p.Pro218=
|
|
ENST00000533800.5:c.403G>A
|
ENSP00000435011.1:p.Ala135Thr
|
|
ENST00000534795.5:c.319+2162G>A
|
|
|
NM_001163817.1:c.1153G>A
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NP_001157289.1:p.Ala385Thr
|
|
NM_001360.2:c.1153G>A , LRG_340t1:c.1153G>A
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NP_001351.2:p.Ala385Thr
|
|
XM_011544777.1:c.1287G>A
|
XP_011543079.1:p.Pro429=
|
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XM_011544777.2:c.1287G>A
|
XP_011543079.1:p.Pro429=
|
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NM_001163817.2:c.1153G>A
|
NP_001157289.1:p.Ala385Thr
|
|
NM_001360.3:c.1153G>A
MANE Select
|
NP_001351.2:p.Ala385Thr
|
|