ENST00000305544.9:c.2573G>T
MANE Select
|
ENSP00000307156.4:p.Gly858Val
|
|
ENST00000305544.8:c.2573G>T
|
ENSP00000307156.4:p.Gly858Val
|
|
ENST00000418109.5:c.2573G>T
|
ENSP00000388325.1:p.Gly858Val
|
|
ENST00000464891.5:n.322G>T
|
|
|
ENST00000477701.1:n.446G>T
|
|
|
ENST00000483057.1:n.173G>T
|
|
|
ENST00000486298.5:n.426-231G>T
|
|
|
NM_002292.3:c.2573G>T
|
NP_002283.3:p.Gly858Val
|
|
XM_005265127.3:c.2573G>T
|
XP_005265184.1:p.Gly858Val
|
|
XM_005265127.4:c.2573G>T
|
XP_005265184.1:p.Gly858Val
|
|
NM_002292.4:c.2573G>T
MANE Select
|
NP_002283.3:p.Gly858Val
|
|