ENST00000394867.9:n.1435G>T
|
|
|
ENST00000688002.1:n.3147G>T
|
|
|
ENST00000688751.1:n.132G>T
|
|
|
ENST00000689792.1:n.900G>T
|
|
|
ENST00000262948.10:c.996G>T
MANE Select
|
ENSP00000262948.4:p.Lys332Asn
|
|
ENST00000262948.9:c.996G>T
|
ENSP00000262948.3:p.Lys332Asn
|
|
ENST00000394867.8:c.705G>T
|
ENSP00000378336.1:p.Lys235Asn
|
|
ENST00000595715.1:n.811G>T
|
|
|
ENST00000597263.5:n.181G>T
|
|
|
ENST00000599021.1:c.106G>T
|
|
|
ENST00000600584.5:n.1556G>T
|
|
|
ENST00000601786.5:n.1297G>T
|
|
|
NM_030662.3:c.996G>T , LRG_750t1:c.996G>T
|
NP_109587.1:p.Lys332Asn
|
|
XM_006722799.2:c.717G>T
|
XP_006722862.1:p.Lys239Asn
|
|
XM_011528133.1:c.426G>T
|
XP_011526435.1:p.Lys142Asn
|
|
XM_017026989.1:c.996G>T
|
XP_016882478.1:p.Lys332Asn
|
|
XM_017026990.1:c.717G>T
|
XP_016882479.1:p.Lys239Asn
|
|
NM_030662.4:c.996G>T
MANE Select
|
NP_109587.1:p.Lys332Asn
|
|