ENST00000264414.9:c.1326A>C
MANE Select
|
ENSP00000264414.4:p.Thr442=
|
|
ENST00000264414.8:c.1326A>C
|
ENSP00000264414.4:p.Thr442=
|
|
ENST00000344951.8:c.1128A>C
|
ENSP00000343601.4:p.Thr376=
|
|
ENST00000409096.5:c.1254A>C
|
ENSP00000387200.1:p.Thr418=
|
|
ENST00000409777.5:c.1254A>C
|
ENSP00000386525.1:p.Thr418=
|
|
ENST00000481135.1:n.622A>C
|
|
|
ENST00000617432.4:c.50A>C
|
ENSP00000477851.1:p.Gln17Pro
|
|
NM_001257197.1:c.1128A>C
|
NP_001244126.1:p.Thr376=
|
|
NM_001257198.1:c.1344A>C
|
NP_001244127.1:p.Thr448=
|
|
NM_003590.4:c.1326A>C
|
NP_003581.1:p.Thr442=
|
|
XM_006712800.2:c.1293A>C
|
XP_006712863.2:p.Thr431=
|
|
XM_011511994.1:c.1179A>C
|
XP_011510296.1:p.Thr393=
|
|
XM_011511995.1:c.1284A>C
|
XP_011510297.1:p.Thr428=
|
|
XM_011511996.1:c.1134A>C
|
XP_011510298.1:p.Thr378=
|
|
XM_011511997.1:c.1026A>C
|
XP_011510299.1:p.Thr342=
|
|
XM_011511994.3:c.1179A>C
|
XP_011510296.1:p.Thr393=
|
|
XM_011511996.2:c.1134A>C
|
XP_011510298.1:p.Thr378=
|
|
NM_003590.5:c.1326A>C
MANE Select
|
NP_003581.1:p.Thr442=
|
|
NM_001257198.2:c.1344A>C
|
NP_001244127.1:p.Thr448=
|
|
NM_001257197.2:c.1128A>C
|
NP_001244126.1:p.Thr376=
|
|