ENST00000394867.9:n.1495G>C
|
|
|
ENST00000688002.1:n.3207G>C
|
|
|
ENST00000688751.1:n.192G>C
|
|
|
ENST00000689792.1:n.960G>C
|
|
|
ENST00000262948.10:c.1056G>C
MANE Select
|
ENSP00000262948.4:p.Lys352Asn
|
|
ENST00000262948.9:c.1056G>C
|
ENSP00000262948.3:p.Lys352Asn
|
|
ENST00000394867.8:c.765G>C
|
ENSP00000378336.1:p.Lys255Asn
|
|
ENST00000597263.5:n.241G>C
|
|
|
ENST00000599021.1:c.166G>C
|
|
|
ENST00000600584.5:n.2505G>C
|
|
|
ENST00000601786.5:n.1357G>C
|
|
|
NM_030662.3:c.1056G>C , LRG_750t1:c.1056G>C
|
NP_109587.1:p.Lys352Asn
|
|
XM_006722799.2:c.777G>C
|
XP_006722862.1:p.Lys259Asn
|
|
XM_011528133.1:c.486G>C
|
XP_011526435.1:p.Lys162Asn
|
|
NM_030662.4:c.1056G>C
MANE Select
|
NP_109587.1:p.Lys352Asn
|
|