ENST00000347401.8:c.1556A>C
|
|
|
ENST00000353578.9:c.8293A>C
|
ENSP00000315873.4:p.Arg2765=
|
|
ENST00000682957.1:c.1038A>C
|
|
|
ENST00000684508.1:n.1178A>C
|
|
|
ENST00000295550.9:c.8911A>C
MANE Select
|
ENSP00000295550.4:p.Arg2971=
|
|
ENST00000295550.8:c.8911A>C
|
ENSP00000295550.4:p.Arg2971=
|
|
ENST00000347401.7:c.7087A>C
|
ENSP00000315609.4:p.Arg2363=
|
|
ENST00000353578.8:c.8293A>C
|
ENSP00000315873.4:p.Arg2765=
|
|
ENST00000409809.5:c.8293A>C
|
ENSP00000386844.1:p.Arg2765=
|
|
ENST00000472056.5:c.7090A>C
|
ENSP00000418285.1:p.Arg2364=
|
|
ENST00000491769.1:n.5353A>C
|
|
|
NM_004369.3:c.8911A>C , LRG_473t1:c.8911A>C
|
NP_004360.2:p.Arg2971=
|
|
NM_057166.4:c.7090A>C
|
NP_476507.3:p.Arg2364=
|
|
NM_057167.3:c.8293A>C
|
NP_476508.2:p.Arg2765=
|
|
XM_005246065.1:c.8311A>C
|
XP_005246122.1:p.Arg2771=
|
|
XM_005246066.1:c.7690A>C
|
XP_005246123.1:p.Arg2564=
|
|
XM_006712253.1:c.8410A>C
|
XP_006712316.1:p.Arg2804=
|
|
XM_011510574.1:c.8908A>C
|
XP_011508876.1:p.Arg2970=
|
|
XM_011510575.1:c.6505A>C
|
XP_011508877.1:p.Arg2169=
|
|
XM_017003304.1:c.6505A>C
|
XP_016858793.1:p.Arg2169=
|
|
XM_024452684.1:c.7690A>C
|
XP_024308452.1:p.Arg2564=
|
|
NM_004369.4:c.8911A>C
MANE Select
|
NP_004360.2:p.Arg2971=
|
|
NM_057166.5:c.7090A>C
|
NP_476507.3:p.Arg2364=
|
|
NM_057167.4:c.8293A>C
|
NP_476508.2:p.Arg2765=
|
|