ENST00000700559.2:c.1134G>T
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ENSP00000515065.2:p.Gln378His
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ENST00000700563.2:c.1134G>T
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ENSP00000515066.2:p.Gln378His
|
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ENST00000700559.1:c.349G>T
|
|
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ENST00000700560.1:n.349G>T
|
|
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ENST00000700561.1:n.475G>T
|
|
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ENST00000700563.1:c.1088G>T
|
|
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ENST00000700564.1:n.1138G>T
|
|
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ENST00000700565.1:n.987G>T
|
|
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ENST00000070846.11:c.1134G>T
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ENSP00000070846.6:p.Gln378His
|
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ENST00000340811.9:c.1134G>T
MANE Select
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ENSP00000342800.5:p.Gln378His
|
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ENST00000070846.10:c.1134G>T
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ENSP00000070846.6:p.Gln378His
|
|
ENST00000340811.8:c.1134G>T
|
ENSP00000342800.4:p.Gln378His
|
|
ENST00000613243.1:c.1134G>T
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ENSP00000478295.1:p.Gln378His
|
|
NM_001005242.2:c.1134G>T
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NP_001005242.2:p.Gln378His
|
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NM_004572.3:c.1134G>T , LRG_398t1:c.1134G>T
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NP_004563.2:p.Gln378His
|
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NM_001005242.3:c.1134G>T
MANE Select
|
NP_001005242.2:p.Gln378His
|
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NM_004572.4:c.1134G>T
|
NP_004563.2:p.Gln378His
|
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