ENST00000298171.7:c.935_936delinsGA
MANE Select
|
ENSP00000298171.2:p.Arg312=
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|
ENST00000636454.1:n.853_854delinsGA
|
|
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ENST00000298171.6:c.935_936delinsGA
|
ENSP00000298171.2:p.Arg312=
|
|
ENST00000541158.6:c.935_936delinsGA
|
ENSP00000441235.2:p.Arg312=
|
|
NM_000369.2:c.935_936delinsGA , LRG_523t1:c.935_936delinsGA
|
NP_000360.2:p.Arg312=
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|
XM_005268037.3:c.935_936delinsGA
|
XP_005268094.1:p.Arg312=
|
|
XM_011537119.1:c.656_657delinsGA
|
XP_011535421.1:p.Arg219=
|
|
XR_245790.3:n.2086+22199_2086+22200delinsTC
|
|
|
XR_429385.2:n.853+22199_853+22200delinsTC
|
|
|
XR_429386.2:n.854+22199_854+22200delinsTC
|
|
|
XR_944075.1:n.865+22199_865+22200delinsTC
|
|
|
XR_944076.1:n.861+22199_861+22200delinsTC
|
|
|
XR_944077.1:n.865+22199_865+22200delinsTC
|
|
|
XR_944078.1:n.865+22199_865+22200delinsTC
|
|
|
XR_944079.1:n.855+22199_855+22200delinsTC
|
|
|
XM_005268037.4:c.935_936delinsGA
|
XP_005268094.1:p.Arg312=
|
|
XM_011537119.2:c.656_657delinsGA
|
XP_011535421.1:p.Arg219=
|
|
XR_001751021.1:n.2753+22199_2753+22200delinsTC
|
|
|
XR_001751022.1:n.2753+22199_2753+22200delinsTC
|
|
|
XR_001751023.1:n.2753+22199_2753+22200delinsTC
|
|
|
XR_944075.3:n.929+22199_929+22200delinsTC
|
|
|
NM_000369.4:c.935_936delinsGA
|
NP_000360.2:p.Arg312=
|
|
NM_000369.5:c.935_936delinsGA
MANE Select
|
NP_000360.2:p.Arg312=
|
|