ENST00000347401.8:c.1528A>G
|
|
|
ENST00000353578.9:c.8265A>G
|
ENSP00000315873.4:p.Lys2755=
|
|
ENST00000682957.1:c.1010A>G
|
|
|
ENST00000684508.1:n.1150A>G
|
|
|
ENST00000295550.9:c.8883A>G
MANE Select
|
ENSP00000295550.4:p.Lys2961=
|
|
ENST00000295550.8:c.8883A>G
|
ENSP00000295550.4:p.Lys2961=
|
|
ENST00000347401.7:c.7059A>G
|
ENSP00000315609.4:p.Lys2353=
|
|
ENST00000353578.8:c.8265A>G
|
ENSP00000315873.4:p.Lys2755=
|
|
ENST00000409809.5:c.8265A>G
|
ENSP00000386844.1:p.Lys2755=
|
|
ENST00000472056.5:c.7062A>G
|
ENSP00000418285.1:p.Lys2354=
|
|
ENST00000491769.1:n.5325A>G
|
|
|
NM_004369.3:c.8883A>G , LRG_473t1:c.8883A>G
|
NP_004360.2:p.Lys2961=
|
|
NM_057166.4:c.7062A>G
|
NP_476507.3:p.Lys2354=
|
|
NM_057167.3:c.8265A>G
|
NP_476508.2:p.Lys2755=
|
|
XM_005246065.1:c.8283A>G
|
XP_005246122.1:p.Lys2761=
|
|
XM_005246066.1:c.7662A>G
|
XP_005246123.1:p.Lys2554=
|
|
XM_006712253.1:c.8382A>G
|
XP_006712316.1:p.Lys2794=
|
|
XM_011510574.1:c.8880A>G
|
XP_011508876.1:p.Lys2960=
|
|
XM_011510575.1:c.6477A>G
|
XP_011508877.1:p.Lys2159=
|
|
XM_017003304.1:c.6477A>G
|
XP_016858793.1:p.Lys2159=
|
|
XM_024452684.1:c.7662A>G
|
XP_024308452.1:p.Lys2554=
|
|
NM_004369.4:c.8883A>G
MANE Select
|
NP_004360.2:p.Lys2961=
|
|
NM_057166.5:c.7062A>G
|
NP_476507.3:p.Lys2354=
|
|
NM_057167.4:c.8265A>G
|
NP_476508.2:p.Lys2755=
|
|