ENST00000264414.9:c.1266G>T
MANE Select
|
ENSP00000264414.4:p.Met422Ile
|
|
ENST00000264414.8:c.1266G>T
|
ENSP00000264414.4:p.Met422Ile
|
|
ENST00000344951.8:c.1068G>T
|
ENSP00000343601.4:p.Met356Ile
|
|
ENST00000409096.5:c.1194G>T
|
ENSP00000387200.1:p.Met398Ile
|
|
ENST00000409777.5:c.1194G>T
|
ENSP00000386525.1:p.Met398Ile
|
|
ENST00000481135.1:n.562G>T
|
|
|
ENST00000617432.4:c.-11G>T
|
ENSP00000477851.1:n.-11G>T
|
|
NM_001257197.1:c.1068G>T
|
NP_001244126.1:p.Met356Ile
|
|
NM_001257198.1:c.1284G>T
|
NP_001244127.1:p.Met428Ile
|
|
NM_003590.4:c.1266G>T
|
NP_003581.1:p.Met422Ile
|
|
XM_006712800.2:c.1233G>T
|
XP_006712863.2:p.Met411Ile
|
|
XM_011511994.1:c.1119G>T
|
XP_011510296.1:p.Met373Ile
|
|
XM_011511995.1:c.1224G>T
|
XP_011510297.1:p.Met408Ile
|
|
XM_011511996.1:c.1074G>T
|
XP_011510298.1:p.Met358Ile
|
|
XM_011511997.1:c.966G>T
|
XP_011510299.1:p.Met322Ile
|
|
XM_011511994.3:c.1119G>T
|
XP_011510296.1:p.Met373Ile
|
|
XM_011511996.2:c.1074G>T
|
XP_011510298.1:p.Met358Ile
|
|
NM_003590.5:c.1266G>T
MANE Select
|
NP_003581.1:p.Met422Ile
|
|
NM_001257198.2:c.1284G>T
|
NP_001244127.1:p.Met428Ile
|
|
NM_001257197.2:c.1068G>T
|
NP_001244126.1:p.Met356Ile
|
|