ENST00000347401.8:c.1480A>G
|
|
|
ENST00000353578.9:c.8217A>G
|
ENSP00000315873.4:p.Val2739=
|
|
ENST00000682957.1:c.962A>G
|
|
|
ENST00000684508.1:n.1102A>G
|
|
|
ENST00000295550.9:c.8835A>G
MANE Select
|
ENSP00000295550.4:p.Val2945=
|
|
ENST00000295550.8:c.8835A>G
|
ENSP00000295550.4:p.Val2945=
|
|
ENST00000347401.7:c.7011A>G
|
ENSP00000315609.4:p.Val2337=
|
|
ENST00000353578.8:c.8217A>G
|
ENSP00000315873.4:p.Val2739=
|
|
ENST00000409809.5:c.8217A>G
|
ENSP00000386844.1:p.Val2739=
|
|
ENST00000472056.5:c.7014A>G
|
ENSP00000418285.1:p.Val2338=
|
|
ENST00000491769.1:n.5277A>G
|
|
|
NM_004369.3:c.8835A>G , LRG_473t1:c.8835A>G
|
NP_004360.2:p.Val2945=
|
|
NM_057166.4:c.7014A>G
|
NP_476507.3:p.Val2338=
|
|
NM_057167.3:c.8217A>G
|
NP_476508.2:p.Val2739=
|
|
XM_005246065.1:c.8235A>G
|
XP_005246122.1:p.Val2745=
|
|
XM_005246066.1:c.7614A>G
|
XP_005246123.1:p.Val2538=
|
|
XM_006712253.1:c.8334A>G
|
XP_006712316.1:p.Val2778=
|
|
XM_011510574.1:c.8832A>G
|
XP_011508876.1:p.Val2944=
|
|
XM_011510575.1:c.6429A>G
|
XP_011508877.1:p.Val2143=
|
|
XM_017003304.1:c.6429A>G
|
XP_016858793.1:p.Val2143=
|
|
XM_024452684.1:c.7614A>G
|
XP_024308452.1:p.Val2538=
|
|
NM_004369.4:c.8835A>G
MANE Select
|
NP_004360.2:p.Val2945=
|
|
NM_057166.5:c.7014A>G
|
NP_476507.3:p.Val2338=
|
|
NM_057167.4:c.8217A>G
|
NP_476508.2:p.Val2739=
|
|