ENST00000534624.6:c.1128G>C
MANE Select
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ENSP00000432083.1:p.Gln376His
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ENST00000227378.7:c.1128G>C
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ENSP00000227378.3:p.Gln376His
|
|
ENST00000453788.6:c.1128G>C
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ENSP00000404372.2:p.Gln376His
|
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ENST00000524552.5:c.-100G>C
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ENSP00000435908.1:n.-100G>C
|
|
ENST00000526110.5:c.1071G>C
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ENSP00000433584.1:p.Gln357His
|
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ENST00000526862.1:n.406G>C
|
|
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ENST00000527983.5:n.1488G>C
|
|
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ENST00000532091.1:n.875G>C
|
|
|
ENST00000532636.5:c.1128G>C
|
ENSP00000437125.1:p.Gln376His
|
|
ENST00000533238.5:n.381-151G>C
|
|
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ENST00000533540.5:c.690G>C
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ENSP00000437189.1:p.Gln230His
|
|
ENST00000534319.5:c.420G>C
|
ENSP00000433316.1:p.Gln140His
|
|
ENST00000534624.5:c.1128G>C
|
ENSP00000432083.1:p.Gln376His
|
|
NM_006597.5:c.1128G>C
|
NP_006588.1:p.Gln376His
|
|
NM_153201.3:c.1128G>C
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NP_694881.1:p.Gln376His
|
|
XM_011542798.1:c.1128G>C
|
XP_011541100.1:p.Gln376His
|
|
NM_006597.6:c.1128G>C
MANE Select
|
NP_006588.1:p.Gln376His
|
|
NM_153201.4:c.1128G>C
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NP_694881.1:p.Gln376His
|
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