ENST00000315491.12:c.1278G>T
MANE Select
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ENSP00000320295.7:p.Gln426His
|
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ENST00000680788.1:n.4699G>T
|
|
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ENST00000315491.11:c.1278G>T
|
ENSP00000320295.7:p.Gln426His
|
|
ENST00000554444.5:c.1062G>T
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ENSP00000451617.1:p.Gln354His
|
|
ENST00000555576.5:c.277+2151G>T
|
ENSP00000452554.1:n.277+2151G>T
|
|
ENST00000555609.5:c.*1363G>T
|
ENSP00000451276.1:n.*1363G>T
|
|
ENST00000556922.1:c.2319G>T
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ENSP00000451560.1:p.Gln773His
|
|
NM_001197181.1:c.1062G>T
|
NP_001184110.1:p.Gln354His
|
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NM_006086.3:c.1278G>T
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NP_006077.2:p.Gln426His
|
|
NM_006086.4:c.1278G>T
MANE Select
|
NP_006077.2:p.Gln426His
|
|
NM_001197181.2:c.1062G>T
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NP_001184110.1:p.Gln354His
|
|