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NM_006767.4:c.55G>C
MANE Select
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NP_006758.2:p.Gly19Arg
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|
ENST00000646124.2:c.55G>C
MANE Select
|
ENSP00000496779.1:p.Gly19Arg
|
|
NM_006767.3:c.55G>C
|
NP_006758.2:p.Gly19Arg
|
|
ENST00000215739.12:c.55G>C
|
ENSP00000215739.8:p.Gly19Arg
|
|
ENST00000414985.5:c.55G>C
|
ENSP00000397247.1:p.Gly19Arg
|
|
ENST00000443265.5:c.55G>C
|
ENSP00000406466.1:p.Gly19Arg
|
|
ENST00000479606.5:n.347-601G>C
|
|
|
ENST00000493460.1:n.130G>C
|
|
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ENST00000493460.2:n.130G>C
|
|
|
ENST00000645935.1:c.55G>C
|
ENSP00000493479.1:p.Gly19Arg
|
|
ENST00000700578.1:c.55G>C
|
ENSP00000515073.1:p.Gly19Arg
|