ENST00000347401.8:c.132G>C
|
|
|
ENST00000353578.9:c.6869G>C
|
ENSP00000315873.4:p.Arg2290Thr
|
|
ENST00000295550.9:c.7487G>C
MANE Select
|
ENSP00000295550.4:p.Arg2496Thr
|
|
ENST00000295550.8:c.7487G>C
|
ENSP00000295550.4:p.Arg2496Thr
|
|
ENST00000347401.7:c.5663G>C
|
ENSP00000315609.4:p.Arg1888Thr
|
|
ENST00000353578.8:c.6869G>C
|
ENSP00000315873.4:p.Arg2290Thr
|
|
ENST00000409809.5:c.6869G>C
|
ENSP00000386844.1:p.Arg2290Thr
|
|
ENST00000472056.5:c.5666G>C
|
ENSP00000418285.1:p.Arg1889Thr
|
|
ENST00000491769.1:n.1741G>C
|
|
|
NM_004369.3:c.7487G>C , LRG_473t1:c.7487G>C
|
NP_004360.2:p.Arg2496Thr
|
|
NM_057166.4:c.5666G>C
|
NP_476507.3:p.Arg1889Thr
|
|
NM_057167.3:c.6869G>C
|
NP_476508.2:p.Arg2290Thr
|
|
XM_005246065.1:c.6887G>C
|
XP_005246122.1:p.Arg2296Thr
|
|
XM_005246066.1:c.6266G>C
|
XP_005246123.1:p.Arg2089Thr
|
|
XM_006712253.1:c.6986G>C
|
XP_006712316.1:p.Arg2329Thr
|
|
XM_011510574.1:c.7484G>C
|
XP_011508876.1:p.Arg2495Thr
|
|
XM_011510575.1:c.5081G>C
|
XP_011508877.1:p.Arg1694Thr
|
|
XM_017003304.1:c.5081G>C
|
XP_016858793.1:p.Arg1694Thr
|
|
XM_024452684.1:c.6266G>C
|
XP_024308452.1:p.Arg2089Thr
|
|
NM_004369.4:c.7487G>C
MANE Select
|
NP_004360.2:p.Arg2496Thr
|
|
NM_057166.5:c.5666G>C
|
NP_476507.3:p.Arg1889Thr
|
|
NM_057167.4:c.6869G>C
|
NP_476508.2:p.Arg2290Thr
|
|