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NM_006767.4:c.1085G>A
MANE Select
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NP_006758.2:p.Arg362Gln
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ENST00000646124.2:c.1085G>A
MANE Select
|
ENSP00000496779.1:p.Arg362Gln
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NM_006767.3:c.1085G>A
|
NP_006758.2:p.Arg362Gln
|
|
ENST00000215739.12:c.1085G>A
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ENSP00000215739.8:p.Arg362Gln
|
|
ENST00000461510.1:n.186G>A
|
|
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ENST00000479606.5:n.1231G>A
|
|
|
ENST00000492480.1:n.141G>A
|
|
|
ENST00000495142.6:n.430G>A
|
|
|
ENST00000497716.5:n.912G>A
|
|
|
ENST00000642151.1:c.916G>A
|
|
|
ENST00000643578.1:n.1107G>A
|
|
|
ENST00000646506.1:n.664G>A
|
|
|
ENST00000700578.1:c.1085G>A
|
ENSP00000515073.1:p.Arg362Gln
|