ENST00000455537.7:c.880G>C
MANE Select
|
ENSP00000408979.2:p.Gly294Arg
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ENST00000674619.1:c.880G>C
|
ENSP00000502270.1:p.Gly294Arg
|
|
ENST00000676081.1:n.26G>C
|
|
|
ENST00000676457.1:c.775G>C
|
ENSP00000501588.1:p.Gly259Arg
|
|
ENST00000286452.5:c.613G>C
|
ENSP00000286452.5:p.Gly205Arg
|
|
ENST00000455537.6:c.880G>C
|
ENSP00000408979.2:p.Gly294Arg
|
|
NM_004984.2:c.880G>C
|
NP_004975.2:p.Gly294Arg
|
|
NM_001354705.1:c.613G>C
|
NP_001341634.1:p.Gly205Arg
|
|
NM_004984.3:c.880G>C
|
NP_004975.2:p.Gly294Arg
|
|
XR_002957324.1:n.1113G>C
|
|
|
NM_004984.4:c.880G>C
MANE Select
|
NP_004975.2:p.Gly294Arg
|
|
NM_001354705.2:c.613G>C
|
NP_001341634.1:p.Gly205Arg
|
|