ENST00000347401.8:c.226A>T
|
|
|
ENST00000353578.9:c.6963A>T
|
ENSP00000315873.4:p.Arg2321Ser
|
|
ENST00000295550.9:c.7581A>T
MANE Select
|
ENSP00000295550.4:p.Arg2527Ser
|
|
ENST00000295550.8:c.7581A>T
|
ENSP00000295550.4:p.Arg2527Ser
|
|
ENST00000347401.7:c.5757A>T
|
ENSP00000315609.4:p.Arg1919Ser
|
|
ENST00000353578.8:c.6963A>T
|
ENSP00000315873.4:p.Arg2321Ser
|
|
ENST00000409809.5:c.6963A>T
|
ENSP00000386844.1:p.Arg2321Ser
|
|
ENST00000472056.5:c.5760A>T
|
ENSP00000418285.1:p.Arg1920Ser
|
|
ENST00000491769.1:n.1835A>T
|
|
|
NM_004369.3:c.7581A>T , LRG_473t1:c.7581A>T
|
NP_004360.2:p.Arg2527Ser
|
|
NM_057166.4:c.5760A>T
|
NP_476507.3:p.Arg1920Ser
|
|
NM_057167.3:c.6963A>T
|
NP_476508.2:p.Arg2321Ser
|
|
XM_005246065.1:c.6981A>T
|
XP_005246122.1:p.Arg2327Ser
|
|
XM_005246066.1:c.6360A>T
|
XP_005246123.1:p.Arg2120Ser
|
|
XM_006712253.1:c.7080A>T
|
XP_006712316.1:p.Arg2360Ser
|
|
XM_011510574.1:c.7578A>T
|
XP_011508876.1:p.Arg2526Ser
|
|
XM_011510575.1:c.5175A>T
|
XP_011508877.1:p.Arg1725Ser
|
|
XM_017003304.1:c.5175A>T
|
XP_016858793.1:p.Arg1725Ser
|
|
XM_024452684.1:c.6360A>T
|
XP_024308452.1:p.Arg2120Ser
|
|
NM_004369.4:c.7581A>T
MANE Select
|
NP_004360.2:p.Arg2527Ser
|
|
NM_057166.5:c.5760A>T
|
NP_476507.3:p.Arg1920Ser
|
|
NM_057167.4:c.6963A>T
|
NP_476508.2:p.Arg2321Ser
|
|