ENST00000347401.8:c.1558G>T
|
|
|
ENST00000353578.9:c.8295G>T
|
ENSP00000315873.4:p.Arg2765Ser
|
|
ENST00000682957.1:c.1040G>T
|
|
|
ENST00000684508.1:n.1180G>T
|
|
|
ENST00000295550.9:c.8913G>T
MANE Select
|
ENSP00000295550.4:p.Arg2971Ser
|
|
ENST00000295550.8:c.8913G>T
|
ENSP00000295550.4:p.Arg2971Ser
|
|
ENST00000347401.7:c.7089G>T
|
ENSP00000315609.4:p.Arg2363Ser
|
|
ENST00000353578.8:c.8295G>T
|
ENSP00000315873.4:p.Arg2765Ser
|
|
ENST00000409809.5:c.8295G>T
|
ENSP00000386844.1:p.Arg2765Ser
|
|
ENST00000472056.5:c.7092G>T
|
ENSP00000418285.1:p.Arg2364Ser
|
|
ENST00000491769.1:n.5355G>T
|
|
|
NM_004369.3:c.8913G>T , LRG_473t1:c.8913G>T
|
NP_004360.2:p.Arg2971Ser
|
|
NM_057166.4:c.7092G>T
|
NP_476507.3:p.Arg2364Ser
|
|
NM_057167.3:c.8295G>T
|
NP_476508.2:p.Arg2765Ser
|
|
XM_005246065.1:c.8313G>T
|
XP_005246122.1:p.Arg2771Ser
|
|
XM_005246066.1:c.7692G>T
|
XP_005246123.1:p.Arg2564Ser
|
|
XM_006712253.1:c.8412G>T
|
XP_006712316.1:p.Arg2804Ser
|
|
XM_011510574.1:c.8910G>T
|
XP_011508876.1:p.Arg2970Ser
|
|
XM_011510575.1:c.6507G>T
|
XP_011508877.1:p.Arg2169Ser
|
|
XM_017003304.1:c.6507G>T
|
XP_016858793.1:p.Arg2169Ser
|
|
XM_024452684.1:c.7692G>T
|
XP_024308452.1:p.Arg2564Ser
|
|
NM_004369.4:c.8913G>T
MANE Select
|
NP_004360.2:p.Arg2971Ser
|
|
NM_057166.5:c.7092G>T
|
NP_476507.3:p.Arg2364Ser
|
|
NM_057167.4:c.8295G>T
|
NP_476508.2:p.Arg2765Ser
|
|