ENST00000394867.9:n.1594A>G
|
|
|
ENST00000688002.1:n.3306A>G
|
|
|
ENST00000688751.1:n.291A>G
|
|
|
ENST00000689792.1:n.1059A>G
|
|
|
ENST00000262948.10:c.1155A>G
MANE Select
|
ENSP00000262948.4:p.Lys385=
|
|
ENST00000262948.9:c.1155A>G
|
ENSP00000262948.3:p.Lys385=
|
|
ENST00000394867.8:c.864A>G
|
ENSP00000378336.1:p.Lys288=
|
|
ENST00000597263.5:n.340A>G
|
|
|
ENST00000599021.1:c.265A>G
|
|
|
ENST00000600584.5:n.2604A>G
|
|
|
ENST00000601786.5:n.1456A>G
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|
|
NM_030662.3:c.1155A>G , LRG_750t1:c.1155A>G
|
NP_109587.1:p.Lys385=
|
|
XM_006722799.2:c.876A>G
|
XP_006722862.1:p.Lys292=
|
|
XM_011528133.1:c.585A>G
|
XP_011526435.1:p.Lys195=
|
|
NM_030662.4:c.1155A>G
MANE Select
|
NP_109587.1:p.Lys385=
|
|