ENST00000348974.5:c.1059A>C
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ENSP00000330021.7:p.Ala353=
|
|
ENST00000394236.9:c.1059A>C
MANE Select
|
ENSP00000377783.3:p.Ala353=
|
|
ENST00000407433.6:c.1014A>C
|
ENSP00000385794.2:p.Ala338=
|
|
ENST00000647936.1:c.1059A>C
|
ENSP00000496822.1:p.Ala353=
|
|
ENST00000648381.1:n.1227A>C
|
|
|
ENST00000648853.1:c.1017A>C
|
ENSP00000497262.1:p.Ala339=
|
|
ENST00000649103.1:c.1158A>C
|
ENSP00000497962.1:n.1158A>C
|
|
ENST00000650591.1:c.1155A>C
|
ENSP00000497376.1:p.Ala385=
|
|
ENST00000394236.7:c.1059A>C
|
ENSP00000377783.3:p.Ala353=
|
|
ENST00000407433.5:c.666A>C
|
ENSP00000385794.1:p.Ala222=
|
|
NM_000313.3:c.1059A>C , LRG_572t1:c.1059A>C
|
NP_000304.2:p.Ala353=
|
|
NM_001314077.1:c.1155A>C , LRG_572t2:c.1155A>C
|
NP_001301006.1:p.Ala385=
|
|
NM_000313.4:c.1059A>C
MANE Select
|
NP_000304.2:p.Ala353=
|
|
NM_001314077.2:c.1155A>C
|
NP_001301006.1:p.Ala385=
|
|