|
NM_006767.4:c.1889G>A
MANE Select
|
NP_006758.2:p.Arg630Gln
|
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ENST00000646124.2:c.1889G>A
MANE Select
|
ENSP00000496779.1:p.Arg630Gln
|
|
NM_006767.3:c.1889G>A
|
NP_006758.2:p.Arg630Gln
|
|
ENST00000215739.12:c.1889G>A
|
ENSP00000215739.8:p.Arg630Gln
|
|
ENST00000415354.6:c.201G>A
|
ENSP00000393765.2:p.Ala67=
|
|
ENST00000415817.2:c.201G>A
|
|
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ENST00000439171.5:c.171G>A
|
|
|
ENST00000452988.5:c.68G>A
|
ENSP00000408789.1:p.Arg23Gln
|
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ENST00000464807.1:n.150G>A
|
|
|
ENST00000479606.5:n.2035G>A
|
|
|
ENST00000491432.5:n.310G>A
|
|
|
ENST00000495142.5:n.505G>A
|
|
|
ENST00000495142.6:n.1522G>A
|
|
|
ENST00000642151.1:c.1720G>A
|
|
|
ENST00000643578.1:n.1911G>A
|
|
|
ENST00000643710.1:n.750G>A
|
|
|
ENST00000646506.1:n.1756G>A
|
|
|
ENST00000700578.1:c.1889G>A
|
ENSP00000515073.1:p.Arg630Gln
|