ENST00000264414.9:c.1345G>C
MANE Select
|
ENSP00000264414.4:p.Asp449His
|
|
ENST00000264414.8:c.1345G>C
|
ENSP00000264414.4:p.Asp449His
|
|
ENST00000344951.8:c.1147G>C
|
ENSP00000343601.4:p.Asp383His
|
|
ENST00000409096.5:c.1273G>C
|
ENSP00000387200.1:p.Asp425His
|
|
ENST00000409777.5:c.1273G>C
|
ENSP00000386525.1:p.Asp425His
|
|
ENST00000481135.1:n.641G>C
|
|
|
ENST00000617432.4:c.69G>C
|
ENSP00000477851.1:p.Met23Ile
|
|
NM_001257197.1:c.1147G>C
|
NP_001244126.1:p.Asp383His
|
|
NM_001257198.1:c.1363G>C
|
NP_001244127.1:p.Asp455His
|
|
NM_003590.4:c.1345G>C
|
NP_003581.1:p.Asp449His
|
|
XM_006712800.2:c.1312G>C
|
XP_006712863.2:p.Asp438His
|
|
XM_011511994.1:c.1198G>C
|
XP_011510296.1:p.Asp400His
|
|
XM_011511995.1:c.1303G>C
|
XP_011510297.1:p.Asp435His
|
|
XM_011511996.1:c.1153G>C
|
XP_011510298.1:p.Asp385His
|
|
XM_011511997.1:c.1045G>C
|
XP_011510299.1:p.Asp349His
|
|
XM_011511994.3:c.1198G>C
|
XP_011510296.1:p.Asp400His
|
|
XM_011511996.2:c.1153G>C
|
XP_011510298.1:p.Asp385His
|
|
NM_003590.5:c.1345G>C
MANE Select
|
NP_003581.1:p.Asp449His
|
|
NM_001257198.2:c.1363G>C
|
NP_001244127.1:p.Asp455His
|
|
NM_001257197.2:c.1147G>C
|
NP_001244126.1:p.Asp383His
|
|