ENST00000382061.5:c.1331T>A
|
ENSP00000371493.4:p.Leu444His
|
|
ENST00000453066.6:c.1331T>A
MANE Select
|
ENSP00000402286.2:p.Leu444His
|
|
ENST00000324015.7:c.1331T>A
|
ENSP00000321853.3:p.Leu444His
|
|
ENST00000382061.4:c.1331T>A
|
ENSP00000371493.4:p.Leu444His
|
|
ENST00000450523.6:c.1139T>A
|
ENSP00000403877.2:p.Leu380His
|
|
NM_000934.3:c.1331T>A , LRG_885t1:c.1331T>A
|
NP_000925.2:p.Leu444His
|
|
NM_001165920.1:c.1331T>A
|
NP_001159392.1:p.Leu444His
|
|
NM_001165921.1:c.1139T>A
|
NP_001159393.1:p.Leu380His
|
|
XM_005256699.3:c.1436T>A
|
XP_005256756.1:p.Leu479His
|
|
XM_005256700.3:c.1343T>A
|
XP_005256757.1:p.Leu448His
|
|
XM_005256701.3:c.1379T>A
|
XP_005256758.2:p.Leu460His
|
|
XM_005256703.3:c.1250T>A
|
XP_005256760.1:p.Leu417His
|
|
XM_005256701.4:c.1379T>A
|
XP_005256758.2:p.Leu460His
|
|
XM_017024765.1:c.1343T>A
|
XP_016880254.1:p.Leu448His
|
|
XM_024450805.1:c.1343T>A
|
XP_024306573.1:p.Leu448His
|
|
NM_000934.4:c.1331T>A
MANE Select
|
NP_000925.2:p.Leu444His
|
|
NM_001165921.2:c.1139T>A
|
NP_001159393.1:p.Leu380His
|
|