|
NM_021939.4:c.587G>A
MANE Select
|
NP_068758.3:p.Ser196Asn
|
|
ENST00000321562.9:c.587G>A
MANE Select
|
ENSP00000317232.4:p.Ser196Asn
|
|
NM_021939.3:c.587G>A , LRG_12t1:c.587G>A
|
NP_068758.3:p.Ser196Asn
|
|
ENST00000321562.8:c.587G>A
|
ENSP00000317232.4:p.Ser196Asn
|
|
ENST00000489591.5:c.441G>A
|
ENSP00000466352.1:p.Gln147=
|
|
ENST00000585664.5:c.407G>A
|
ENSP00000468703.1:p.Ser136Asn
|
|
ENST00000706683.1:c.587G>A
|
ENSP00000516497.1:p.Ser196Asn
|
|
XM_011525099.1:c.587G>A
|
XP_011523401.1:p.Ser196Asn
|
|
XM_011525099.3:c.587G>A
|
XP_011523401.1:p.Ser196Asn
|
|
XM_011525100.1:c.314G>A
|
XP_011523402.1:p.Ser105Asn
|
|
XM_011525100.2:c.314G>A
|
XP_011523402.1:p.Ser105Asn
|