ENST00000264414.9:c.1334G>T
MANE Select
|
ENSP00000264414.4:p.Ser445Ile
|
|
ENST00000264414.8:c.1334G>T
|
ENSP00000264414.4:p.Ser445Ile
|
|
ENST00000344951.8:c.1136G>T
|
ENSP00000343601.4:p.Ser379Ile
|
|
ENST00000409096.5:c.1262G>T
|
ENSP00000387200.1:p.Ser421Ile
|
|
ENST00000409777.5:c.1262G>T
|
ENSP00000386525.1:p.Ser421Ile
|
|
ENST00000481135.1:n.630G>T
|
|
|
ENST00000617432.4:c.58G>T
|
ENSP00000477851.1:p.Val20Leu
|
|
NM_001257197.1:c.1136G>T
|
NP_001244126.1:p.Ser379Ile
|
|
NM_001257198.1:c.1352G>T
|
NP_001244127.1:p.Ser451Ile
|
|
NM_003590.4:c.1334G>T
|
NP_003581.1:p.Ser445Ile
|
|
XM_006712800.2:c.1301G>T
|
XP_006712863.2:p.Ser434Ile
|
|
XM_011511994.1:c.1187G>T
|
XP_011510296.1:p.Ser396Ile
|
|
XM_011511995.1:c.1292G>T
|
XP_011510297.1:p.Ser431Ile
|
|
XM_011511996.1:c.1142G>T
|
XP_011510298.1:p.Ser381Ile
|
|
XM_011511997.1:c.1034G>T
|
XP_011510299.1:p.Ser345Ile
|
|
XM_011511994.3:c.1187G>T
|
XP_011510296.1:p.Ser396Ile
|
|
XM_011511996.2:c.1142G>T
|
XP_011510298.1:p.Ser381Ile
|
|
NM_003590.5:c.1334G>T
MANE Select
|
NP_003581.1:p.Ser445Ile
|
|
NM_001257198.2:c.1352G>T
|
NP_001244127.1:p.Ser451Ile
|
|
NM_001257197.2:c.1136G>T
|
NP_001244126.1:p.Ser379Ile
|
|