ENST00000309755.9:c.1458A>C
MANE Select
|
ENSP00000312397.4:p.Gly486=
|
|
ENST00000309755.8:c.1458A>C
|
ENSP00000312397.4:p.Gly486=
|
|
ENST00000447439.6:n.1514A>C
|
|
|
ENST00000504208.5:c.*342A>C
|
ENSP00000423585.1:n.*342A>C
|
|
ENST00000506491.5:c.1212A>C
|
ENSP00000424828.1:p.Gly404=
|
|
ENST00000506873.5:n.981A>C
|
|
|
ENST00000508657.5:c.1362A>C
|
ENSP00000422099.1:p.Gly454=
|
|
ENST00000509694.1:n.251A>C
|
|
|
NM_001257194.1:c.1362A>C
|
NP_001244123.1:p.Gly454=
|
|
NM_001257195.1:c.1212A>C
|
NP_001244124.1:p.Gly404=
|
|
NM_017415.2:c.1458A>C
|
NP_059111.2:p.Gly486=
|
|
NM_017415.3:c.1458A>C
MANE Select
|
NP_059111.2:p.Gly486=
|
|
NM_001257195.2:c.1212A>C
|
NP_001244124.1:p.Gly404=
|
|