ENST00000282516.13:c.5236G>T
MANE Select
|
ENSP00000282516.8:p.Asp1746Tyr
|
|
ENST00000652901.1:c.5236G>T
|
ENSP00000499536.1:p.Asp1746Tyr
|
|
ENST00000282516.12:c.5236G>T
|
ENSP00000282516.8:p.Asp1746Tyr
|
|
ENST00000448238.2:c.5236G>T
|
ENSP00000406266.2:p.Asp1746Tyr
|
|
ENST00000621733.1:c.1-43793G>T
|
ENSP00000480694.1:n.1-43793G>T
|
|
NM_015384.4:c.5236G>T
|
NP_056199.2:p.Asp1746Tyr
|
|
NM_133433.3:c.5236G>T
|
NP_597677.2:p.Asp1746Tyr
|
|
XM_005248280.2:c.5236G>T
|
XP_005248337.1:p.Asp1746Tyr
|
|
XM_005248282.3:c.4492G>T
|
XP_005248339.2:p.Asp1498Tyr
|
|
XM_006714467.2:c.5236G>T
|
XP_006714530.1:p.Asp1746Tyr
|
|
XM_006714468.1:c.5038G>T
|
XP_006714531.1:p.Asp1680Tyr
|
|
XM_011514014.1:c.4855G>T
|
XP_011512316.1:p.Asp1619Tyr
|
|
XM_011514015.1:c.5236G>T
|
XP_011512317.1:p.Asp1746Tyr
|
|
XM_005248280.3:c.5236G>T
|
XP_005248337.1:p.Asp1746Tyr
|
|
XM_005248282.5:c.4576G>T
|
XP_005248339.3:p.Asp1526Tyr
|
|
XM_006714468.2:c.5038G>T
|
XP_006714531.1:p.Asp1680Tyr
|
|
XM_017009329.1:c.5236G>T
|
XP_016864818.1:p.Asp1746Tyr
|
|
XM_017009330.2:c.3619G>T
|
XP_016864819.1:p.Asp1207Tyr
|
|
XM_017009331.1:c.3610G>T
|
XP_016864820.1:p.Asp1204Tyr
|
|
NM_133433.4:c.5236G>T
MANE Select
|
NP_597677.2:p.Asp1746Tyr
|
|
NM_015384.5:c.5236G>T
|
NP_056199.2:p.Asp1746Tyr
|
|